documents: FDA-2017-D-5625-0001

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2017-D-5625-0001 FDA FDA-2017-D-5625 Recommendations for Dual 510(k) and Clinical Laboratory Improvement Amendments Waiver by Application Studies; Draft Guidance for Industry and Food and Drug Administration Staff; Availability Notice Notice of Availability 2017-11-29T05:00:00Z 2017 11 2017-11-29T05:00:00Z 2018-01-30T04:59:59Z 2018-01-14T03:27:10Z 2017-25774 0 0 0900006482cbbd24

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