documents: FDA-2011-D-0476-0010

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-0476-0010 FDA FDA-2011-D-0476 Guidance for Industry and Staff; Enforcement Policy for Premarket Notification Requirements for Certain In Vitro Diagnostic and Radiology Devices Other Guidance 2011-12-20T05:00:00Z 2011 12 2011-12-20T05:00:00Z   2020-04-29T14:40:32Z   0 0 0900006480f8692a

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