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Baxter Receives 510(k) Clearance From FDA For V-Link With VitalShield, New Antimicrobial Intravascular Technology
Date:11/9/2007

unt=prnewswire&PageName=QUOTE&Ticker=BAX" onClick="var s=s_gi(s_account); var hd1 = document.getElementById('headline'); s.tl(this,'o',getLinkName('Company Sanpshot'));" >BAX). Baxter International Inc., through its subsidiaries, assists healthcare professionals and their patients with the treatment of complex medical conditions, including cancer, hemophilia, immune disorders, kidney disease and trauma. The company applies its expertise in medical devices, pharmaceuticals and biotechnology to make a meaningful difference in patients' lives.

This release includes forward-looking statements concerning our plans to launch V-Link with VitalShield in the U.S. and other global markets, the introduction of new products to help reduce risks associated with IV therapy and promote increased security and confidence in the delivery of IV medications and the ability of healthcare professionals to combat pathogens and make healthcare facilities safer for patients and clinicians. These statements are based on assumptions about many important factors, including the following, which could cause actual results to differ materially from those in the forward-looking statements: our ability to make V-Link with VitalShield and other new products available for sale in accordance with our plans; customer and market acceptance of V-Link with VitalShield and other new products; clinician practices and procedures; future actions by the FDA and other regulatory bodies and government authorities with respect to the company's infusion pumps and other new products; and other risks identified in Baxter International Inc.'s most recent filing on Form 10-Q and other SEC filings, all of which are available on the company's website. The company does not undertake to update its forward-looking statements.


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