Yorkey v. Diab

601 F.3d 1279, 94 U.S.P.Q. 2d (BNA) 1435, 2010 U.S. App. LEXIS 7165, 2010 WL 1337338
CourtCourt of Appeals for the Federal Circuit
DecidedApril 7, 2010
Docket2008-1577
StatusPublished
Cited by37 cases

This text of 601 F.3d 1279 (Yorkey v. Diab) is published on Counsel Stack Legal Research, covering Court of Appeals for the Federal Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Yorkey v. Diab, 601 F.3d 1279, 94 U.S.P.Q. 2d (BNA) 1435, 2010 U.S. App. LEXIS 7165, 2010 WL 1337338 (Fed. Cir. 2010).

Opinion

*1281 MICHEL, Chief Judge.

Appellant Thomas J. Yorkey (“Yorkey”) appeals from a decision of the Board of Patent Appeals and Interferences (the “Board”) denying his motion seeking invalidity of claims 16-18 and 21 of Appellees Mohamed K. Diab, Esmaiel Kiani-Azraby Jany, Ibrahim M. Elfadel, Rex J. McCarthy, Walter M. Weber, and Robert A. Smith’s (collectively “Diab”) U.S. Patent Application Ser. No. 09/110,542 (the “Diab application”) on the grounds that the claims fail to comply with the written description requirement of 35 U.S.C. § 112, ¶ 1. Yorkey also appeals from the Board’s ruling that he failed to establish a prima facie case of actual reduction to practice and the Board’s consequent award of priority to the Diab application over Yorkey’s U.S. Patent No. 5,645,060 (the “Yorkey patent”). Because we find that that the asserted claims of the Diab application meet the written description requirement of § 112, we affirm the Board’s denial of Yorkey’s motion. However, we reverse the Board’s finding that Yorkey failed to establish a prima facie case of actual reduction to practice and remand the case to the Board for further proceedings.

PROCEDURAL HISTORY

The patent and patent application at issue in this appeal claim inventions for measuring the concentration of oxygen in blood. Yorkey is named as the inventor of the Yorkey patent, which issued on July 8, 1997 and was based on U.S. Application Ser. No. 08/490,315, filed on June 14, 1995. The patent was subsequently assigned to Nellcor Puritan Bennet, Inc. (“Nellcor”) which is the party in interest. Diab is the named inventor of the Diab application filed on July 6, 1998, which claims priority in turn from U.S. Application Ser. Nos. 08/859,837 (filed May 16, 1997) and 08/320,-154 (filed October 7, 1994); the party in interest in the Diab application is Masimo Corporation (“Masimo”). An interference (No. 105,471) was declared by the Board on July 18, 2006, and Yorkey was declared the junior party.

Two counts were declared in the interference: Count 1 included claims 1, 2, 8, and 12-16 of the Yorkey patent and 15, 19, and 20 of the Diab application; Count 2 embraced claims 3-5, 7, 10, 11, and 17 of the Yorkey patent and claims 16-18 and 21 of the Diab application.

During the motions phase of the interference, Yorkey filed four motions, all of which were denied by the Board. At issue in the instant appeal is the Board’s denial of Yorkey’s motion seeking to have Diab’s claims corresponding to Counts 1 and 2 denied for failure to comply with the written description requirement of 35 U.S.C. § 112, ¶ 1.

Yorkey also appeals the Board’s holding that he failed to establish a prima facie case that he had reduced his invention to practice prior to Diab’s benefit date of October 7,1994.

BACKGROUND

The technology at issue in this case is medical instrumentation designed for the measurement of physiological signals. Specifically, the inventions claimed by the Yorkey patent and the Diab application are directed at the noninvasive measurement of the amount of oxygen in the blood of a patient (“pulse oximetry”) which is an indicator of the healthful function of the pulmonary and cardiovascular systems responsible for the delivery of oxygen to the body’s tissues.

A major problem in the detection of blood oxygen saturation is the presence of ambient interference (“noise”) which can obscure the measurement of blood oxygen saturation by introducing extraneous signals into the recorded measurement. Improving the signal-to-noise ratio is a central concern in the design of biomedical *1282 instrumentation for detecting physiological signals, which are often weak when compared to background noise. Certain types of noise can be removed by the use of passive or active bandpass or notch filters (which filter out signals of frequencies that are outside the range of the signals that the device is attempting to detect). However, if the signal and the noise are coincident within the same range of frequencies, simple frequency filtering is insufficient and a means of separating the signal from the noise in which it is embedded must be contrived.

Prior technologies for the suppression of noise have relied upon the direct subtraction of noise from the signal. However, the claims at issue in the interference are directed to a method of noise filtering that does not directly subtract motion-induced noise from the detected signal. This method relies upon two assumptions: (1) that the amount of actual motion is the same for each of the two separate intensity signals measured by the probe (typically one signal is measured from transmitted light in the red wavelengths of the visible light spectrum and one in the infrared wavelengths); and (2) the motion component portions of the detected signals are proportionate. The relevant portion of Count I is set forth below:

A method for measuring saturation of a blood constituent in a patient comprising the steps of:
irradiating said patient with electromagnetic radiation of two discrete, different wavelengths;
sensing an intensity of said radiation for each of said wavelengths after it passes through a portion of said patient to produce first and second intensity signals including motion components; and
determining said saturation by mathematically manipulating said first and second intensity signals without subtracting said motion components and with the assumptions that
i) an amount of motion is the same at the same time for each of said intensity signals, and
ii) the motion components of said intensity signals are proportional to one another.

Count 2 is similar to Count I, but includes additional steps directed to determining oxygen saturation in the presence of motion-induced interference. Claim 16 of the Diab application is representative of the claims embraced by Count 2; the claim recites identical language to Count 1 recited above, and continues after the ellipsis:

A method for measuring saturation of a blood constituent in a patient comprising the steps of:
taking the logarithm of each representation of said first and second intensity signals;
removing signal portions outside a known band of interest to create first and second filtered signals; equating the first filtered signal of the first intensity signal to s + n, where n is the portion of the signal due to motion and s is the portion of the signal not due to motion;
equating the second filtered signal of the second intensity signal to ras + rTO, where ra, is a ratio indicative of saturation;
expressing said representations as a matrix;
using said matrix to determine ra, by assuming s and n are uncorrelated; and determining said saturation from r a. 2

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601 F.3d 1279, 94 U.S.P.Q. 2d (BNA) 1435, 2010 U.S. App. LEXIS 7165, 2010 WL 1337338, Counsel Stack Legal Research, https://law.counselstack.com/opinion/yorkey-v-diab-cafc-2010.