documents: FDA-2021-N-0009-0001

Regulatory documents from Regulations.gov including rules, proposed rules, notices, and supporting materials.

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id agency_id docket_id title document_type subtype posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id
FDA-2021-N-0009-0001 FDA FDA-2021-N-0009 Making Permanent Regulatory Flexibilities Provided During the COVID–19 Public Health Emergency by Exempting Certain Medical Devices From Premarket Notification Requirements; Request for Information, Research, Analysis, and Public Comment on Opportunities for Further Science and Evidence-Based Reform of Section 510(k) Program Notice Requests for Information (RFI) 2021-01-15T05:00:00Z 2021 1 2021-01-15T05:00:00Z 2021-03-16T03:59:59Z 2024-11-06T23:43:54Z 2021-00787 1 0 09000064849f406a

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