Regulations.gov document

Electronic Submission Template for Medical Device 510(k) Submissions; Draft Guidance for…

Notice · FDA-2021-D-0872 · posted Sep 29, 2021

Key facts

Document ID FDA-2021-D-0872-0001
Title Electronic Submission Template for Medical Device 510(k) Submissions; Draft Guidance for Industry and Food and Drug Administration Staff; Availability
Document type Notice
Subtype Notice of Availability
Agency FDA
Docket FDA-2021-D-0872
Posted Sep 29, 2021
Federal Register citation 86 FR 53965
FR document number 2021-21135
Comment period opens Sep 29, 2021
Comments due Nov 30, 2021
Effective date Sep 29, 2021

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  • 1–9 Pages
  • No Open for comment
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