Posted By
Peggy McLaughlin
08-Nov-2018 11:16
Found In
Egroup:
Regulatory Open Forum
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I wanted to bring the following proposed rule to folks' attention. www.federalregister.gov/documents/2018/09/13/2018-19865/medical-device-submissions-amending-premarket-regulations-that-require-multiple-copies-and-specify Published in September, Marjorie Schulman noted today on the Special 510(k) Pilot ...
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