Baxter Healthcare Corporation announced today that it has received clearance from the U.S. Food and Drug Administration (FDA) on its COLLEAGUE infusion pump 510(k) pre-market notification. The company is preparing to modify pumps currently in the market and will soon submit manufacturing and service documentation to FDA in advance of deploying upgrades to U.S. COLLEAGUE infusion pumps. [click link for full article]
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Source: Medical Devices News From Medical News Today