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withdrawn,object_id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-0628-0004,FDA,FDA-2018-N-0628,03 - eCopy Proposed Rule Regulatory Impact Analysis,Supporting & Related Material,Background Material,2018-09-13T04:00:00Z,2018,9,,,2018-09-13T16:17:23Z,,0,0,09000064836e8426
FDA-2018-N-0628-0002,FDA,FDA-2018-N-0628,01 - Reference 1-Guidance for eCopy Program for Medical Device Submissions,Supporting & Related Material,Background Material,2018-09-13T04:00:00Z,2018,9,,,2018-09-13T16:15:36Z,,0,0,09000064836e8424
FDA-2018-N-0628-0003,FDA,FDA-2018-N-0628,02 - Reference 2-Electronic Submissions Gateway,Supporting & Related Material,Background Material,2018-09-13T04:00:00Z,2018,9,,,2018-09-13T16:16:30Z,,0,0,09000064836e8425
FDA-2018-N-0628-0001,FDA,FDA-2018-N-0628,"Medical Device Submissions: Amending Premarket Regulations That
Require Multiple Copies and Specify Paper Copies To Be Allowed in
Electronic Format",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2018-09-13T04:00:00Z,2018,9,2018-09-13T04:00:00Z,2018-12-13T04:59:59Z,2018-12-12T02:03:47Z,2018-19865,0,0,09000064836e65a5