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Baxter Int'l, Inc. v. Carefusion Corp.
AMY J. ST. EVE, United States District Judge:
Defendants CareFusion Corporation and Beckton, Dickinson, and Company (collectively, "CareFusion" or "Defendants") seek to dismiss two claims brought by Plaintiff Baxter International, Inc. ("Baxter"). (R.34). Baxter's First Amended Complaint alleges that Defendants infringed three patents relating to medical infusion pumps: U.S. Patent Nos. 5,764,034 ('034 Patent); 5,782,805 ('805 Patent); and 6,321,560 ('560 Patent). (R.29). Defendants now move to dismiss Count I ('034 Patent) and Count III ('560 Patent) pursuant to Federal Rule of Civil Procedure 12(b)(6) for failure to recite patent eligible subject matter under 35 U.S.C. § 101. For the following reasons, the Court denies Defendants' motion.
The '034 Patent, entitled "Battery Gauge For A Battery Operated Infusion Pump" was filed on April 10, 1996. (R.29-1, '034 Patent at 1). The '034 Patent lists two inventors, George Bowman and Grace Esche, and is assigned to Baxter. (Id.). The '034 Patent is directed to an infusion pump capable of estimating the amount of time left on a battery by monitoring both the voltage available from the battery, and the amount of current flowing from the battery. (Id., col. 2: 14-16, 20-23). The summary of the '034 Patent recites: "[t]he present invention provides a medical infusion pump which incorporates cost-effective, sensitive battery monitoring." (Id., col. 2: 11-13). The summary further discloses an electric circuit which enables a "sampling technique [that] alternates between sampling battery voltage and sampling current drain." (Id., col. 2: 25-28). "A method is then applied to the sampling signals by a microprocessor which determines the amount of time left under battery power." (Id., col. 2: 28-30). The specification recites that the "invention also provides several troubleshooting alert, alarm and failure messages" to health care providers. (Id., col. 8: 15-16). The alert condition includes "a battery low alert, which indicates that the auxiliary battery has less than a predetermined amount of infusion time left." (Id., col. 8: 29-32). The alarm condition "indicates that the auxiliary battery charge has diminished below the level necessary to continue infusion." (Id., col. 8: 34-35).
The independent claims of the '034 Patent state:
(Id., col. 15: 36-50).
(Id., col. 15-16: 64-17).
(Id., col. 16: 24-39).
(Id., col. 16-18: 50-3).
The '560 Patent, entitled "Method and Apparatus For Automatically Controlling The Level of Medication" was filed on February 10, 1999. (R.29-3, '560 Patent at 1). The '560 Patent lists three inventors, Tuan Bui, Doron Levitas, and Stephen L. Axel, and is assigned to Baxter. (Id.). The '560 Patent is directed to "a method and apparatus for automatically adjusting the medication level for a patient . . . based on the patient's pain intensity." (Id., col. 1: 6-10).
The claimed method and apparatus address a need for "automatically adjusting the medication level in response to input from a patient regarding his pain level, side effects and impairment of functionalities, without having to contact the caregiver or physician." (Id., col. 2: 39-43). In particular, the specification discloses "a method and apparatus which captures relevant information pertaining to pain level, side effects and patient impairment and automatically adjusts the amount of medication, within a pre-determined level selected by the patient's physician." (Id., col. 2: 52-56).
The physician or caregiver first programs the pump for a specific patient, after which point "a pain relief algorithm . . . modifies the PCA treatment in response to input regarding the patient's pain level, side effects and function impairment." (Id., col. 2-3: 59-5). The infusion pump detects pain level by storing the number of pain medication requests the patient makes over a prescribed period of time, or by querying the patient directly. (Id. col. 3: 7-14). Similarly, either the patient—through responses to specific queries—or the health care provider may program into the infusion pump information relating to (i) side effects and/or (ii) the impairment of patient functionality. (Id. col. 3: 18-32). "After completion of inputting all data, the data is processed by the algorithm, and the patient's PCA medication rate is conformed to the algorithm or adjusted if indicated by the algorithm." (Id. col. 3: 33-36).
The independent claims of the '560 Patent state:
(Id., col. 14: 6-20).
(Id., col. 14-15: 47-6).
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