documents: FDA-2018-N-0628-0020

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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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2018-N-0628-0020 FDA FDA-2018-N-0628 Medical Device Submissions: Amending Premarket Regulations That Require Multiple Copies and Specify Paper Copies To Be Required in Electronic Format Rule Final Rule 2019-12-16T05:00:00Z 2019 12 2019-12-16T05:00:00Z   2019-12-16T16:22:23Z 2019-27047 0 0 090000648421276f

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