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FDA releases description and timeline of initiatives for improving the 510(k) program

31 January 2011

Medical Device Alert

On Wednesday, January 19, 2011, the Food and Drug Administration's (FDA) Center for Devices and Radiological Health (CDRH) released its 510(k) and Science Report Recommendations outlining actions that the agency will implement in 2011 to improve the 510(k) process.



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