FDA to hold meeting on IOM's 510(k) report in September

08/16/2011 | Clinica (subscription required)

The FDA is scheduled to conduct a public meeting in Maryland on Sept. 16 to discuss an Institute of Medicine report recommending the replacement of the agency's 510(k) clearance process for medical devices. The agency also set a Sept. 30 deadline for public comments on the IOM's recommendations.

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