Hewlett-Packard Co. v. Boston Scientific Corp.

77 F. Supp. 2d 189, 1999 U.S. Dist. LEXIS 19089, 1999 WL 1103343
CourtDistrict Court, D. Massachusetts
DecidedNovember 30, 1999
DocketCiv.A. 99-10244-PBS
StatusPublished
Cited by7 cases

This text of 77 F. Supp. 2d 189 (Hewlett-Packard Co. v. Boston Scientific Corp.) is published on Counsel Stack Legal Research, covering District Court, D. Massachusetts primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Hewlett-Packard Co. v. Boston Scientific Corp., 77 F. Supp. 2d 189, 1999 U.S. Dist. LEXIS 19089, 1999 WL 1103343 (D. Mass. 1999).

Opinion

MEMORANDUM AND ORDER

SARIS, District Judge.

I. INTRODUCTION

Plaintiff Hewlett-Packard Company (“HP”) brings this action 1 against defendant Boston Scientific Corporation (“BSC”) alleging that BSC unlawfully monopolized, or attempted to monopolize, the intravascular ultrasound (“IVUS”) catheter and console markets in the United States, in violation of Section 2 of the Sherman Antitrust Act, 15 U.S.C. § 2, and state law. An IVUS catheter is a flexible tube-like device used in conjunction with a console to obtain sonographic images of arteries. HP also seeks a declaratory judgment that it is no longer obligated to make payments under a licensing agreement which the two companies entered into pursuant to a consent decree required by the Federal Trade Commission (“FTC”) as a condition to allowing BSC’s merger with two other medical technology companies.

BSC has filed a motion to dismiss all counts pursuant to Fed.R.Civ.P. 12(b)(6) on the grounds, inter alia, that the antitrust claim is facially deficient because HP failed to allege: (1) that BSC has current monopoly power in the catheter or console markets in the United States; or (2) that BSC committed predatory acts that could reasonably be interpreted as causing antitrust injury to competition. After hearing and a review of the excellent briefing by both sides, the motion is DENIED.

II. FACTUAL BACKGROUND

When all reasonable inferences are drawn in the non-movant’s favor, HP’s complaint alleges the following facts:

*192 A. The Products: Catheters and Consoles

IVUS catheters are medical devices that are used to diagnose and treat cardiovascular ailments. They are flexible tube-shaped objects that are inserted into a blood vessel. A transducer, located at the forward end of the catheter, generates and transmits ultrasound waves. These waves reflect off the arterial walls, and a receiver measures the amount of returned energy. The catheter compares the transmitted and received energy and sends a signal to a console that displays a 360 degree image of the blood vessel. The image allows physicians to assess the amount of plaque deposits in blood vessels.

There are two types of IVUS catheters. Phased array catheters use several stationary transducers to create a 360 degree image of the blood vessel. Mechanical eathetei's also create a 360 degree image, but do so with a single transducer that is spun by an external motor drive unit. This case centers around mechanical catheters.

B. Market Conditions Prior to 1995

BSC, headquartered in Natick, Massachusetts, develops and manufactures medical products. HP’s headquarters is in Palo Alto, California, and its Medical Products Group is located in Andover, Massachusetts. Both companies have long been participants in IVUS markets — BSC sold catheters and HP sold consoles. Until 1995, they had a cooperative history and on occasion have engaged in joint ventures to design BSC catheters specifically to operate on HP consoles. As of mid-1994, BSC and Cardiovascular Imaging Systems, Inc. (“CVIS”) were the market leaders with respect to the development, manufacture, and sale of IVUS catheters. BSC held 40% of that market, and CVIS held 50%. The market for IVUS consoles was equally concentrated — CVIS controlled 40% and HP controlled 50%.

In August 1994, BSC dramatically shifted the balance of power by seeking to acquire CVIS. Three months later, BSC took steps to acquire SCIMED Life Systems, Inc. (“SCIMED”), which was preparing to enter the IVUS catheter market within the next two to three years.

Believing that BSC’s acquisitions would lessen competition and create monopoly power in the IVUS catheter market, in January 1995 the Federal Trade Commission filed suit against BSC for violation of the Clayton Act, 15 U.S.C. § 45, and the Federal Trade Commission Act, 15 U.S.C. §§ 18 & 21. The FTC sought an injunction to prevent the CVIS acquisition.

C.The Licensing Agreement

As part of settlement negotiations with the FTC, BSC sought a suitable competitor in the IVUS catheter market. On February 21, 1995, the company entered into a licensing agreement granting HP the right to use BSC’s IVUS technology (“Licensed Technology”) in conjunction with the manufacture and sale of certain products (“Licensed Products”).

The licensing agreement defined Licensed Technology as all BSC, SCIMED, and CVIS patents used for the “development, manufacture and sale of Licensed Products ... and all existing know-how” relating to the manufacture, sale, and distribution of those products. Licensed Products included “ultrasound imaging catheters, imaging cores and imaging guide wires which are designed for diagnostic or therapeutic use, or both, in the human heart and/or in the human coronary and peripheral vascular system.”

The Licensed Products definition also referenced Exhibit A, stating that it “includes and is no narrower than the collective claims of the patents ... listed on Exhibit A.” Among several patents listed on Exhibit A was BSC’s “pullback patent.” 2 This technology allows physicians *193 to retrieve an inserted catheter at a fixed rate of speed, enabling the physician to measure plaque accumulations more accurately.

The licensing agreement also included an “open interface” provision that required both parties to ensure that their consoles were able to be used with the other party’s existing catheters. Each party assumed a responsibility to “cooperate ... in furthering this open interface objective,” but retained the option of upgrading its consoles. To facilitate this provision, prior to introducing a new IVUS product, the parties agreed to share technical information relating to new products.

The licensing agreement also contained an “interim supply commitment,” which was designed to allow HP to compete in the catheter market while developing its own line of catheters. BSC agreed to supply HP with all BSC catheters at a below market price (average manufacturing cost plus 40%) for resale by HP. The agreement also required BSC, immediately after acquiring CVIS, to introduce its new “Spy” catheter, which was specifically developed for use with HP consoles.

In exchange for the right to use BSC’s technology, HP agreed to pay a substantial fee. The parties agreed that one-third of the total fee was to be paid within 30 days of the agreement’s effective date. The remaining fee was to be paid in three equal installments payable in May 1998, 2000, and 2002. To date, HP has made the initial payment and the May 1998 installment.

D. The FTC Consent Order

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77 F. Supp. 2d 189, 1999 U.S. Dist. LEXIS 19089, 1999 WL 1103343, Counsel Stack Legal Research, https://law.counselstack.com/opinion/hewlett-packard-co-v-boston-scientific-corp-mad-1999.