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FDA To Up Postmarket Regulation Of Medical Devices

By Erin Marie Daly (November 10, 2006, 12:00 AM EST) -- In a bid to quell escalating concerns over medical device regulation, the U.S. Food and Drug Administration on Thursday jumped into action, revealing plans to bolster the way it monitors the safety of products such as stents, pacemakers, and implantable defibrillators after they reach the marketplace....

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