Koninklijke Philips Electronics N.V. et al v. Zoll Medical Corporation
Filing
465
Judge Nathaniel M. Gorton: ORDER entered. MEMORANDUM AND ORDER: "Accordingly, as previously ruled in the Order of this Court entered on November 6, 2013 (Docket No. 447 ): 1) Plaintiff's Motion for Summary Judgment that (1) the '187 Patent Claims are Invalid as Anticipated, or, in the Alternative, (2) Philips's Accused Products Do Not Infringe the '187 Patent (Docket No. 219 ) is DENIED; 2) Plaintiff's Motion for Summary Judgment of Invalidity of the Asserted Claims of the '526 Patent (Docket No. 223 ) is DENIED; 3) Plaintiff's Motion for Summary Judgment of No Inequitable Conduct (Docket No. 227 ) is DENIED; 4) Defendant's Motion for Summary Judgment of Laches (Docket No. 231 ) is DEN IED; 5) Defendant's Motion for Summary Judgment that (1) No Asserted Claim is Entitled to a Priority Date Before May 10, 1994; (2) Asserted Claims 25, 41, 42, 43, 67-72 of the '374 Patent and Claims 1-7 of the '460 Patent are Invalid for Anticipation; and (3) Asserted Claims 66 and 73 are not Infringed (Docket No. 232 ) is DENIED; 6) Defendant's Motion for Summary Judgment of Non-Infringement of Waveform Patents ('879, '905, '978, and '454 Patents) (Do cket No. 236 ) is DENIED;7) Defendant's Motion for Summary Judgment of Invalidity for Lack of Written Description of Certain Claims of the '212 and '454 Patents (Docket No. 237 ) is DENIED; 8) Plaintiff's Motion for Order to Pre clude ZOLL's Reliance on Documents Not Produced as Required by Fed. R. Civ. P. 26(a) (Docket No. 272 ) is DENIED AS MOOT; 9) The Joint Motion to Dismiss Remaining Claims with Prejudice (Docket No. 369 ) is ALLOWED. So ordered."(Moore, Kellyann)
United States District Court
District of Massachusetts
KONINKLIJKE PHILIPS N.V. AND
PHILIPS ELECTRONICS NORTH
AMERICA CORPORATION,
Plaintiff,
v.
ZOLL MEDICAL CORPORATION,
Defendant.
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Civil Action No.
10-11041-NMG
MEMORANDUM & ORDER
GORTON, J.
Philips Electronics North America Corporation and its
parent company Koninklijke Philips, N.V. (collectively,
“Philips”) brought suit against defendant ZOLL Medical
Corporation (“ZOLL”) in June, 2010.
Philips alleges that ZOLL
infringed fifteen of its patents that relate to various
components of automated external defibrillators.
ZOLL filed a
complaint against Philips one month later in which it alleged
that Philips infringed five of ZOLL’s patents.
The cases were
consolidated in September, 2011, and trial is scheduled to begin
on December 2, 2013.
The parties’ seven motions for summary judgment (Dockets
No. 219, 223, 227, 231, 232, 236 and 237) were denied by a Court
Order entered on November 6, 2013, “with memorandum and order to
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follow.”
The parties’ joint motion to dismiss certain claims
with prejudice (Docket No. 369) was, however, allowed.
The
Court now publishes the subject memorandum and order.
I.
Legal Standard for Resolving Summary Judgment Motions
The role of summary judgment is “to pierce the pleadings
and to assess the proof in order to see whether there is a
genuine need for trial.” Mesnick v. Gen. Elec. Co., 950 F.2d
816, 822 (1st Cir. 1991) (quoting Garside v. Osco Drug, Inc.,
895 F.2d 46, 50 (1st Cir. 1990)). The burden is on the moving
party to show, through the pleadings, discovery and affidavits,
“that there is no genuine issue as to any material fact and that
the moving party is entitled to judgment as a matter of law.”
Fed. R. Civ. P. 56(c).
A fact is material if it “might affect the outcome of the
suit under the governing law.” Anderson v. Liberty Lobby, Inc.,
477 U.S. 242, 248 (1986). “Factual disputes that are irrelevant
or unnecessary will not be counted.” Id.
A genuine issue of
material fact exists where the evidence with respect to the
material fact in dispute “is such that a reasonable jury could
return a verdict for the nonmoving party.” Id.
Once the moving party has satisfied its burden, the burden
shifts to the non-moving party to set forth specific facts
showing that there is a genuine, triable issue. Celotex Corp. v.
Catrett, 477 U.S. 317, 324 (1986).
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The Court must view the
entire record in the light most favorable to the non-moving
party and make all reasonable inferences in that party's favor.
O'Connor v. Steeves, 994 F.2d 905, 907 (1st Cir. 1993).
Summary
judgment is appropriate if, after viewing the record in the nonmoving party's favor, the Court determines that no genuine issue
of material fact exists and that the moving party is entitled to
judgment as a matter of law.
II.
Plaintiff’s Motion for Summary Judgment that (1) the ‘187
Patent Claims are Invalid as Anticipated, or, in the
Alternative, (2) Philips’s Accused Products Do Not Infringe
the ‘187 Patent
A.
Background
ZOLL’s ‘187 patent is directed to a “semi-automatic
defibrillator with heart rate alarm driven by shock advisory
algorithm.”
The “heart rate alarm circuit” described in the
‘187 patent is characterized by inputs that “comprise an
averaged QRS rate and the shock advisory indication.”
This
Court held in its Markman Order that it was clear from that
claim language that both inputs are required.
Heart rate alarm circuits in prior art defibrillators were
activated by either the heart rate (“averaged QRS rate”) or a
shock advisory to indicate to the operator whether the
electrocardiogram shows an abnormal heart rhythm of the sort
that can be corrected by defibrillation shock.
For instance,
the heart rate alarm circuit in the Marquette 1500 is capable of
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receiving an averaged QRS rate in manual mode and a shock
advisory indication in semi-automatic mode but not both at the
same time.
ZOLL will contend at trial that two of Philips’s products,
the MRx and XL defibrillators, infringe the ‘187 patent because
they have as inputs both an averaged QRS rate and a shock
advisory indication when operated in semi-automatic mode.
Philips disagrees and maintains that a user of those devices can
receive a shock advisory indication or a heart rate alarm, but
not both.
According to Philips, the issue boils down to whether the
“heart rate alarm circuit” disclosed in ZOLL’s ‘187 patent
requires both inputs at the same time or not.
It contends that
it will prevail regardless of what interpretation the Court
ultimately adopts.
B.
Anticipation
Philips maintains that if the “heart rate alarm circuit” is
construed as not necessarily receiving average QRS rate and
shock advisory indication inputs at the same time, then the ‘187
patent was anticipated by the prior art Marquette 1500.
1.
Legal Standard
Section 102(e) of the Patent Act provides that an invention
is not patentable if it was described in a previously issued
patent and is therefore “anticipated” by that earlier invention.
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Parties that seek to establish invalidity by anticipation bear
an “especially heavy burden.” Koito Mfg. Co. v. Tum-Key-Tech,
LLC, 381 F.3d 1142, 1151 (Fed. Cir. 2004).
To prove invalidity
by anticipation, the movant must show that
every element and limitation of the claim was
previously described in a single prior art reference,
either expressly or inherently, so as to place a
person of ordinary skill in possession of the
invention.
Sanofi-Synthelabo v. Apotex, Inc., 550 F.3d 1075, 1082 (Fed.
Cir. 2008).
Furthermore,
differences between the prior art reference and a
claimed invention, however slight, invoke the question
of obviousness, not anticipation.
Net MoneyIN, Inc. v. VeriSign, Inc., 545 F.3d 1359, 1371 (Fed.
Cir. 2008).
Anticipation is a question of fact and thus summary
judgment of invalidity is proper only “if no reasonable jury
could find that the patent is not anticipated.” Telemac Cellular
Corp. v. Topp Telecom, Inc., 247 F.3d 1316, 1327 (Fed. Cir.
2001).
2.
Application
The Court finds that Philips has failed to carry its
“especially heavy burden” of proving invalidity by anticipation
at this stage in the litigation as a reasonable jury could find
that the patent was not anticipated by the Marquette 1500 prior
art reference.
In particular, Philips has not accounted for the
differences in circuitry between the prior art and ‘187 patent.
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The evidence, viewed in the light most favorable to ZOLL, is
that the Marquette 1500 is incapable of receiving “dual inputs”
in semi-automatic mode, whereas the claimed term at issue
involves a semi-automatic defibrillator with a circuit that is
capable of receiving two different kinds of inputs.
C.
Non-infringement
In the alternative, Philips argues that if the ‘187 patent
requires that the circuit receive both inputs at the same time,
then its accused products do not infringe because they are
incapable of receiving both inputs at the same time.
1.
Legal Standard
An infringement analysis requires 1) the Court to
determine, as a matter of law, the meaning and scope of the
patent claims asserted to be infringed and 2) the trier of fact
to compare the properly construed claims to the device accused
of infringing. Markman v. Westview Instruments, Inc., 52 F.3d
967, 976 (Fed. Cir. 1995) (en banc), aff'd, 517 U.S. 370 (1996).
Summary judgment of non-infringement is appropriate where
on the correct claim construction, no reasonable jury
could have found infringement on the undisputed facts
or when all reasonable factual inferences are drawn in
favor of the patentee.
Netword, LLC v. Centraal Corp., 242 F.3d 1347, 1353 (Fed. Cir.
2001).
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2.
Application
The Court declines to enter summary judgment because its
Markman Order does not construe the “heart rate alarm circuit”
disclosed in the ‘187 patent to require simultaneous inputs.
Moreover, the Court finds that there is a genuine issue of
material fact as to whether Philips’s products receive both QRSbased and shock advisory inputs while in semi-automatic mode.
Philips asserts that the QRS-based algorithm is only operational
in manual mode and never operates at the same time as the shock
advisory algorithm.
ZOLL responds that the QRS-based algorithm
is never disabled in the MRx and XL defibrillators and therefore
operates in the “background” when the accused products are used
in semi-automatic mode.
While the Court is skeptical of ZOLL’s
claim that the fact that the QRS-based algorithm is always
running is sufficient to show that it is received as an input,
that is a matter for the jury to determine at trial.
III. Plaintiff’s Motion for Summary Judgment of Invalidity of
the Asserted Claims of the ‘526 Patent
A.
Background
ZOLL’s ‘526 patent is directed to defibrillation
electrodes, which are gel-covered plates that are placed on the
patient’s chest.
Prior art electrodes were designed to have
very low electrical resistance (what is known as “low
impedance”) in order to maximize the defibrillation energy
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delivered to the patient.
This design came at a cost: in
particular, low-impedance electrodes were believed to lead to
high electrical current levels at the edges of the plate and gel
which increased the risk of patients experiencing such
discomfort as stinging or burning.
In contrast, the ‘526 patent teaches that a gel-covered
electrode with relatively high impedance (i.e. greater than 1Ω)
reduces the risk of patient discomfort without decreasing the
therapeutic benefits of a defibrillation shock.
In particular,
the patent calls for
a layer of electrolytic gel comprising a concentration
of an electrolyte that produces a combination series
resistance of two of said electrodes, when measured
with the electrodes configured in a series circuit
with a 50Ω resistance, and with the electrolytic gel
layer of each electrode in contact with that of the
other electrode, that is greater than 1Ω when a 200
Joule defibrillation pulse is discharged into the
series circuit.
In other words, the patent teaches that two electrodes are
placed facing each other so that their gel layers are touching.
A defibrillation pulse is then delivered through the electrodes,
and the resistance of the electrode is measured.
If the
measured resistance is greater than 1Ω, it is high enough to
meet the claims and a product that satisfied that criteria would
therefore infringe.
The central issue raised by Philips’s motion is how that 1Ω
resistance is to be measured.
Philips claims that the ‘526
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patent specification is fatally “indefinite” because it fails to
provide any “meaningful guidance” to a person of ordinary skill
in the art with respect to testing parameters, specifically 1)
the temperature of the testing environment, 2) the number of
shocks used and 3) the age of the tested electrode.
Philips
contends that those parameters are important because, without
further guidance, it is possible that an electrode could
infringe when tested in one environment but not infringe if
tested in a different environment.
ZOLL responds that the issues Philips raises are red
herrings because only temperature is a true test condition and a
person skilled in the art would know to run the tests under
indoor room temperature.
It contends that the other parameters
are irrelevant because infringement is measured at the point of
sale and Philips neither sells old electrodes nor electrodes
that have already delivered a half-dozen or more shocks.
B.
Legal Standard
A patent’s specification must be sufficiently “definite” in
that it must “conclude with one or more claims particularly
pointing out and distinctly claiming the subject matter which
the applicant regards as his invention.” 35 U.S.C. § 112.
That
requirement ensures that patent claims will be “sufficiently
precise to permit a potential competitor to determine whether or
not he is infringing.” Amgen Inc. v. Hoechst Marion Roussel,
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Inc., 314 F.3d 1313, 1342 (Fed. Cir. 2003) (internal quotation
marks omitted).
Thus, a claim is considered indefinite if a person of
ordinary skill in the art could not determine if a particular
composition infringes based on the specification. Geneva Pharm.,
Inc. v. GlaxoSmithKline PLC, 349 F.3d 1373, 1384 (Fed. Cir.
2003).
Absolute clarity is not necessary.
Rather, only claims
that are “not amenable to construction” or “insolubly ambiguous”
are indefinite. Datamize, LLC v. Plumtree Software, Inc., 417
F.3d 1342, 1347 (Fed. Cir. 2005).
Moreover, the fact that a
person of ordinary skill in the art would have to engage in some
experimentation to determine the scope of the claim does not
render the claim indefinite, so long as the experimentation is
not “undue”. Exxon Research & Eng’g Co. v. United States, 265
F.3d 1371, 1379 (Fed. Cir. 2001).
The Federal Circuit has explained that indefiniteness is a
question of law. Microprocessor Enhancement Corp. v. Tex.
Instruments Inc., 520 F.3d 1367, 1374 (Fed. Cir. 2008).
To the
extent that this legal conclusion entails questions of fact, the
party claiming invalidity by way of indefiniteness must prove
those facts by clear and convincing evidence. Tech. Licensing
Corp. v. Videotek, Inc., 545 F.3d 1316, 1339 (Fed. Cir. 2008).
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C.
Application
The Court finds that Philips has failed to make the
requisite clear and convincing showing of indefiniteness.
Quite
simply, there is no suggestion that a person of ordinary skill
in the art would not know to test at room temperature.
Instead,
Philips’s argument boils down to whether or not testing at
various temperatures within that range will result in a
measurement of over 1Ω.
For instance, Philips’s expert measured
a resistance of 0.92Ω in a 28 degrees Celsius environment and
1.36Ω at 18 degrees Celsius.
ZOLL maintains that Philips’s
expert used inferior equipment and therefore the results should
be disregarded.
Ultimately, the issue of whether proper testing
methods were used is a question of fact that is more
appropriately resolved by the jury at trial than by the Court at
the summary judgment stage. See ADC Telecomm., Inc. v.
Switchcraft, Inc., 281 F. App’x 989, 992 (Fed. Cir. 2008).
IV.
Plaintiff’s Motion for Summary Judgment of No Inequitable
Conduct
Philips also moves for summary judgment of no inequitable
conduct against ZOLL.
ZOLL alleges that Philips engaged in
inequitable conduct by making a false declaration with respect
to the self-test patents and by failing to disclose material
information to the patent examiner with respect to the waveform
patents.
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A.
Legal Standard
Inequitable conduct is a defense to patent infringement
that, if established, bars enforcement of a patent. Therasense,
Inc. v. Becton, Dickinson & Co., 649 F.3d 1276, 1286 (Fed. Cir.
2011).
ZOLL must prove, by clear and convincing evidence, that
Philips misrepresented or made a deliberate decision to withhold
known material information with the specific intent to deceive
the United States Patent and Trademark Office (“the PTO”). Id.
at 1287, 1290.
To meet the clear and convincing evidence
standard, Philips’s specific intent to deceive the PTO must be
“the single most reasonable inference able to be drawn from the
evidence.” Id. at 1290.
B.
Application
The Court finds that, given the disputed issues of fact, a
reasonable jury could find, but would not be required to find,
that the single most reasonable inference is that Philips acted
with the specific intent to deceive the PTO.
centers on two factual disputes:
Philips’s motion
first, whether Carl Morgan’s
declaration about the publication date of the VivaLink brochure
demonstrated a specific intent to deceive the PTO on a material
issue and, second, whether the disclosures of Philips’s
predecessor-in-interest to the PTO were made with an intent to
deceive.
Both factual disputes involve dueling witness
statements which a jury could choose to believe or not.
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As a
result, the issue is not susceptible to summary judgment and
Philips’s motion will be denied.
V.
Defendant’s Motion for Summary Judgment of Laches
A.
Background
Philips’s relevant waveform patents were issued between
1997 and 2000 while its patents related to self-testing and CPR
instruction were issued between 1998 and 2002.
Philips
initiated litigation related to all of those patents in 2002 and
the final case was resolved in 2007.
In 2008, Philips began to
negotiate with ZOLL to resolve licensing issues and, after the
negotiations failed to produce an agreement, it filed the
instant lawsuit in 2010.
ZOLL has moved for summary judgment of laches on the
grounds that Philips waited 11 years after ZOLL first marketed
and sold the biphasic waveform technology and nine years after
ZOLL first marketed and sold a defibrillator with the allegedly
infringing features to bring an infringement suit.
B.
Legal Standard
Laches is an equitable defense that may bar a party from
relief if its delay in bringing the claim was 1) unreasonable
and inexcusable from the time when the plaintiff had actual or
constructive notice of its potential claim and 2) resulted in
injury or prejudice to the opposing party. A.C. Aukerman Co. v.
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R.L. Chaides Const. Co., 960 F.2d 1020, 1034–35 (Fed. Cir.
1992).
Prejudice can be evidentiary or economic.
In the patent context, a statutory presumption of laches
arises if a preponderance of the evidence reveals that the
patentee delayed filing suit without excuse for more than six
years after actual or constructive knowledge of the defendant's
alleged infringing activity. Id. at 1034–36.
Even if the
presumption is rebutted, unreasonable delay and prejudice may
still bar a plaintiff’s claim. Id. at 1038.
As an equitable
defense, however, laches is not applied mechanically.
Rather,
laches
is
not
established
by
undue
delay
and
prejudice.
Those factors merely lay the foundation
for the trial court’s exercise of discretion.
When
there is evidence of other factors which would make it
inequitable to recognize the defense despite undue
delay and prejudice, the defense may be denied.
Id. at 1036.
Because the laches defense is “fact-intensive,”
summary judgment will often be inappropriate. See, e.g.,
Rockwell Int’l Corp. v. SDL, Inc., 103 F. Supp. 2d 1192, 1196
(N.D. Cal. 2000).
C.
Application
ZOLL argues that Philips had constructive notice of
potential infringement in 1999 when ZOLL first marketed and sold
a defibrillator using biphasic waveform technology and that
Philips’s subsequent litigation against different parties does
not excuse its delay in filing suit against ZOLL.
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Philips disputes ZOLL’s timeline and asserts that any
delay was reasonable and should be excused.
It contends that it
first became aware of potential infringement in 2008 and, to the
extent that it was aware of ZOLL’s infringement earlier than
2008, the delay in filing suit was reasonable because of ongoing
litigation and its 2008 negotiations with ZOLL.
The most important dispute concerns whether Philips’s
undisputed awareness of ZOLL’s use of biphasic waveform
technology also constituted constructive notice that ZOLL was
violating Philips’s waveform patents.
ZOLL argues that Philips’
awareness put it on notice of potential violations.
Philips
responds that many technologies use biphasic waveforms such that
their use by ZOLL would not put Philips on notice of a potential
infringement.
This highly technical dispute is not susceptible
to summary judgment because it involves disputed facts and
questions of witness credibility.
Accordingly, the Court will
deny ZOLL’s motion for summary judgment of laches.1
1
Because the Court will deny defendant ZOLL’s motion for summary
judgment of laches (Docket No. 231), it is unnecessary for the Court
to address plaintiff Philips’s motion to preclude ZOLL from relying
on certain documents in its laches motion (Docket No. 272). That
motion will therefore be denied as moot.
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VI.
Defendant’s Motion for Summary Judgment that (1) No
Asserted Claim is Entitled to a Priority Date Before May
10, 1994; (2) Asserted Claims 25, 41, 42, 43, 67-72 of the
‘374 Patent and Claims 1-7 of the ‘460 Patent are Invalid
for Anticipation; and (3) Asserted Claims 66 and 73 are not
Infringed
As an initial matter, the parties’ joint motion to dismiss
certain claims (Docket No. 369) narrows the scope of the instant
motion.
The Court will limit its analysis to arguments
pertaining to claims 41, 42, 43, 66, 67, 68 and 73 of the ‘374
patent and claim 7 of the ‘460 patent.
A.
Priority Dates for the ‘374 and ‘460 Patents
The main issue underlying this motion is whether Philips is
entitled to claim an earlier priority date for its ‘374 and ‘460
patents.
The four relevant dates for the purposes of the
instant motion are:
(1)
May 18, 1993: the date on which the ‘631 application
(“the first application”) was filed. Carl Morgan was
named as the sole inventor. It disclosed a
defibrillator that performs periodic, automatic selftests through a microprocessor and without user
intervention and then indicates the results on a
visual status indicator.
(2)
March 11, 1994: the date on which the prior art “Wiley
patent” application was filed. It disclosed an
external defibrillator capable of performing selftests in order to monitor the operational status of
the defibrillator and to indicate when some or all of
the defibrillator is inoperable. The defibrillator
disclosed by the Wiley patent detects when it is in a
“quiescent” state and conducts automatic self-tests
without user intervention.
(3)
May 10, 1994: the date on which the ‘374 application
(“the second application”) was filed as a
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“continuation-in-part” to the first application. It
named five additional inventors and included some new
material. The Wiley patent was not cited during
prosecution of this patent.
(4)
April 16, 1997: the date on which the ‘460 application
was filed. The parties agree that the ‘460 patent
includes a specification that is substantially similar
to the ‘374 application.
In this case, the parties dispute whether Philips is
entitled to claim the filing date of the ‘631 application as the
priority date for the ‘374 and ‘460 patents such that the Wiley
patent is not prior art as to those patents. ZOLL seeks summary
judgment that the earliest priority date that Philips can claim
for its ‘374 and ‘460 patents is May 10, 1994 and therefore
several of its claims under those patents are invalid as
anticipated by prior art.
1.
Legal Standard
Section 102(e) of the Patent Act provides that a patent is
invalid as anticipated if the underlying invention was described
in a published United States patent application filed before the
invention’s effective reference date.
However, an inventor can
“swear behind” the prior art patent application and claim the
“priority date” of an earlier-filed application if
(1) the written description of the earlier filed
application discloses the invention claimed in the
later filed application to satisfy the requirements of
§ 112; (2) the applications have at least one common
inventor; (3) the later application is filed before
the issuance or abandonment of the earlier filed
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application; and (4) the later application contains a
reference to the earlier filed application.
In re NTP, Inc., 654 F.3d 1268, 1277 (Fed. Cir. 2011).
The issue here is whether the written description in the
earlier-filed ‘631 application discloses the inventions claimed
in the later-filed ‘374 and ‘460 patents.
The “written
description” requirement in the context of a CIP application
holds that the earlier-filed application must describe the
invention in “sufficient detail” such that one skilled in the
art could “clearly conclude” that the inventor “possessed” the
invention as of the earlier filing date. Lockwood v. Am.
Airlines, Inc., 107 F.3d 1565, 1572 (Fed. Cir. 1997).
Whether the inventor “possessed” the invention as of the
earlier filing date is a question of fact. Ariad Pharms., Inc.
v. Eli Lilly & Co., 598 F.3d 1336, 1351 (Fed. Cir. 2010) (en
banc).
The Federal Circuit has noted that the amount of detail
required to demonstrate possession as of an earlier date depends
on the context. Id.
Factors relevant to the inquiry include
“the nature and scope of the claims and . . . the complexity and
predictability of the relevant technology.” Id.
The inquiry requires courts to proceed on a claim-by-claim
basis because each claim in the later-filed application must be
supported by the earlier application.
Subject matter that
arises for the first time in a CIP application does not receive
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the earlier filing date of the “parent” application. Augustine
Med., Inc. v. Gaymar Indus., Inc., 181 F.3d 1291, 1302 (Fed.
Cir. 1999).
As a result, it is possible for some claims in a
CIP application to receive the benefit of an earlier filing date
while others do not. Id.
As always, the challenged patent is entitled to a
presumption of validity and “the burden of persuasion to the
contrary is and remains on the party asserting invalidity.”
Ralston Purina Co. v. Far-Mar-Co, Inc., 772 F.2d 1570, 1573
(Fed. Cir. 1985).
Where, as here, the U.S. Patent and Trademark
Office did not make an explicit finding as to the correct filing
date for the CIP application, the challenger bears the initial
burden of establishing a prima facie case of invalidity by clear
and convincing evidence.
Specifically, it must show that prior
art that anticipated the invention disclosed in the CIP
application predated the filing of the CIP application. See
PowerOasis, Inc. v. T-Mobile USA, Inc., 522 F.3d 1299, 1303-06
(Fed. Cir. 2008).
If that requirement is met, the burden shifts
to the patent-holder to come forward with evidence to prove that
it is entitled to an earlier filing date. Id.
It should produce
“sufficient evidence and argument to show that an ancestor [to
the CIP patent] contains a written description that supports all
of the limitations of . . . the claim[s] being asserted.” Tech.
Licensing Corp., 545 F.3d at 1327.
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If the patent-holder
produces sufficient evidence, the burden again shifts to the
challenger to overcome the presumption of validity with
convincing evidence that the patentee is not entitled to the
earlier date. Id. at 1328.
2.
Application
The Court will not enter summary judgment on this matter.
The parties’ experts disagree about whether a person of ordinary
skill in the art would have understood Philips to “possess” the
disputed claims at the time the ‘631 application was filed.
ZOLL has not carried its burden of presenting clear and
convincing evidence that Philips is not entitled to the earlier
filing date and therefore is not entitled to summary judgment in
its favor.
As the priority date remains in dispute, summary
judgment of anticipation is unwarranted.
B.
Non-Infringement of Claims 66 and 73 of ‘374 Patent
ZOLL also argues that its accused products do not infringe
because claims 66 and 73 of the ‘374 patent require
“recalibrating” as part of the self-testing process and ZOLL’s
products do not recalibrate during self-tests.
Philips has,
however, presented evidence that suggests that ZOLL’s products
undergo a process where “bad” data is replaced with “good” data.
After construing the facts in favor of Philips as the non-moving
party, the Court finds that a reasonable jury could determine
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that such a process entailed recalibration and therefore
declines to enter summary judgment in ZOLL’s favor.
VII. Defendant’s Motion for Summary Judgment of Non-Infringement
of Waveform Patents (‘879, ‘905, ‘978, and ‘454 Patents)
ZOLL also seeks summary judgment of non-infringement on the
grounds that its accused products involve a fundamentally
different method for generating defibrillation shock waveforms
for a particular patient than the methods claimed by Philips’s
waveform patents.
As described above, summary judgment of non-infringement is
appropriate where, “on the correct claim construction, no
reasonable jury could have found infringement” on the undisputed
facts or when all reasonable factual inferences are drawn in
favor of the patentee.” Netword, LLC, 242 F.3d at 1353.
There are several factual disputes that preclude the entry
of summary judgment in ZOLL’s favor.
ZOLL, for example,
contests vigorously Philips’s claim that ZOLL’s technologies
infringe on the ‘879 patent’s method of “measuring a patient’s
impedance during the discharge step.”
ZOLL argues that although
its defibrillators “calculate” patient impedance “during” the
discharge step, they measure the current at a different moment
such that any measurement of patient impedance does not occur
“during” the discharge step.
Defibrillator technology is
undoubtedly complex but the Court finds it squarely within the
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realm of possibility that a reasonable jury could find that, in
fact, ZOLL’s “calculating” infringes on Philips’ patent covering
the act of “measuring.”
As a result, it will not grant summary
judgment on this motion.
VIII. Defendant’s Motion for Summary Judgment of Invalidity for
Lack of Written Description of Certain Claims of the ‘212
and ‘454 Patents
First, the Court notes that, for the most part, this motion
involves claims that were dismissed as a result of the parties’
joint motion.
Philips will not assert claims 8-10 and 12 with
respect to the ‘212 patent at trial and therefore the Court will
not address ZOLL’s arguments with respect to those claims here.
With respect the ‘454 patent, the joint motion to dismiss
stipulates that claims 51, 53 and 54 will be at issue at trial.
Claim 52 is not mentioned in the motion.
The Court therefore
assumes that only claim 51 of the ‘454 patent is at issue.
A.
Legal Standard
At issue in this motion is whether claim 51 of the ‘454
patent satisfies the “written description” requirement described
in the first paragraph of § 112 of the Patent Act.
That
provision states that
The specification shall contain a written description
of the invention, and of the manner and process of
making and using it, in such full, clear, concise, and
exact terms as to enable any person skilled in the art
to which it pertains, or with which it is most nearly
connected, to make and use the same, and shall set
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forth the best mode contemplated by the inventor of
carrying out his invention.
35 U.S.C. § 112.
To satisfy the written description
requirement, “the description must ‘clearly allow persons of
ordinary skill in the art to recognize that [the inventor]
invented what is claimed.’ ” Ariad Pharms., 598 F.3d at 1351
(quoting Vas–Cath, Inc. v. Mahurkar, 935 F.2d 1555, 1562–63
(Fed. Cir. 1991)).
The written description inquiry is a question of fact. Id.
(citing Ralston Purina, 772 F.2d at 1575).
At the summary
judgment stage, Philips is entitled to a presumption that the
‘454 patent is valid. 35 U.S.C. § 282.
ZOLL may of course rebut
that presumption but must do so with clear and convincing
evidence. Microsoft Corp. v. i4i Ltd. P’ship, 131 S. Ct. 2238,
2242 (2011).
B.
Application
The parties disagree about whether claim 51 of the ‘454
patent satisfies the written description requirement.
It is
undisputed that the ‘454 patent resulted from an application
that amended claims in an earlier application.
Furthermore, it
is undisputed that the following language was added to the ‘454
application as part of claim 51 and did not appear in the
earlier version:
removing the additional impedance from the electrical
circuit if the electrical parameter is within a
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defined
step.
range
prior
to
the
end
of
the
discharging
ZOLL argues that this part of the claim is not supported by the
specification of ‘454.
Yet Philips points to language in the
‘454 specification that states that
If the peak current is below a circuit safety
threshold, then switch 66 is closed to take safety
resistor 64 out of the circuit.
A reasonable jury could find that the written description is
satisfactory based on that language.
While ZOLL may be able to
proffer evidence showing that such provisions do not support
claim 51 at trial, it has not made a sufficiently clear and
convincing showing to warrant summary judgment in its favor.
ORDER
Accordingly, as previously ruled in the Order of this Court
entered on November 6, 2013 (Docket No. 447):
1)
Plaintiff’s Motion for Summary Judgment that (1) the
‘187 Patent Claims are Invalid as Anticipated, or, in
the Alternative, (2) Philips’s Accused Products Do Not
Infringe the ‘187 Patent (Docket No. 219) is DENIED;
2)
Plaintiff’s Motion for Summary Judgment of Invalidity
of the Asserted Claims of the ‘526 Patent (Docket No.
223) is DENIED;
3)
Plaintiff’s Motion for Summary Judgment of No
Inequitable Conduct (Docket No. 227) is DENIED;
4)
Defendant’s Motion for Summary Judgment of Laches
(Docket No. 231) is DENIED;
5)
Defendant’s Motion for Summary Judgment that (1) No
Asserted Claim is Entitled to a Priority Date Before
May 10, 1994; (2) Asserted Claims 25, 41, 42, 43, 6772 of the ‘374 Patent and Claims 1-7 of the ‘460
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Patent are Invalid for Anticipation; and (3) Asserted
Claims 66 and 73 are not Infringed (Docket No. 232) is
DENIED;
6)
Defendant’s Motion for Summary Judgment of NonInfringement of Waveform Patents (‘879, ‘905, ‘978,
and ‘454 Patents) (Docket No. 236) is DENIED;
7)
Defendant’s Motion for Summary Judgment of Invalidity
for Lack of Written Description of Certain Claims of
the ‘212 and ‘454 Patents (Docket No. 237) is DENIED;
8)
Plaintiff’s Motion for Order to Preclude ZOLL’s
Reliance on Documents Not Produced as Required by Fed.
R. Civ. P. 26(a) (Docket No. 272) is DENIED AS MOOT;
9)
The Joint Motion to Dismiss Remaining Claims with
Prejudice (Docket No. 369) is ALLOWED.
So ordered.
/s/ Nathaniel M. Gorton
Nathaniel M. Gorton
United States District Judge
Dated November 19, 2013
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