FDA device unit's webcast focuses on 510(k) process overhaul

08/31/2010 | Modern Healthcare (free registration)

A webcast from the FDA's Center for Devices and Radiological Health held on Tuesday aimed to address medical-device firms' and other industry experts' concerns and discuss several proposals for overhauling the 510(k) process. "By increasing the predictability and reliability of the review process, we can ensure patient safety and foster innovation," said Jeffrey Shuren, director of the agency's device center.

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Modern Healthcare (free registration)

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