documents: FDA-2011-D-0652-0032

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2011-D-0652-0032 FDA FDA-2011-D-0652 The 510(k) Program: Evaluating Substantial Equivalence in Premarket Notifications; Guidance for Industry and Food and Drug Administration Staff; Availability Notice Notice of Availability 2014-07-28T04:00:00Z 2014 7 2014-07-28T04:00:00Z   2014-10-26T01:01:37Z 2014-17666 0 0 09000064817e60aa

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