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FDA Releases Highly-Anticipated Working Group Reports on 510(k) Program, New Science

August 2010

Medical Device Alert

On Wednesday, 4 August 2010, the Food and Drug Administration's (FDA) Center for Devices and Radiological Health (CDRH) released the highly-anticipated preliminary reports of two internal agency working groups evaluating ways to improve the premarket notification 510(k) program, and ways to incorporate advances in scientific knowledge into the regulatory decision-making process.

Read "FDA Releases Highly-Anticipated Working Group Reports on 510(k) Program, New Science

The team

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