Regulations.gov document

The 510(k) Third Party Review Program; Guidance for Industry, Food and Drug Administration…

Notice · FDA-2016-D-2565 · posted Mar 12, 2020

Key facts

Document ID FDA-2016-D-2565-0019
Title The 510(k) Third Party Review Program; Guidance for Industry, Food and Drug Administration Staff, and Third Party Review Organizations; Availability
Document type Notice
Subtype Notice of Availability
Agency FDA
Docket FDA-2016-D-2565
Posted Mar 12, 2020
Federal Register citation 85 FR 14489
FR document number 2020-05080
Comment period opens Mar 12, 2020
Effective date Mar 12, 2020

At a glance

  • 1–9 Pages
  • 10–99 Public comments on this docket

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