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withdrawn,object_id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-2012-D-0530-0038,FDA,FDA-2012-D-0530,Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Q-Submission Program for Medical Devices,Notice,30 Day Proposed Information Collection,2022-12-22T05:00:00Z,2022,12,2022-12-22T05:00:00Z,2023-01-24T04:59:59Z,2022-12-22T14:51:41Z,2022-27815,0,0,090000648554d616
FDA-2012-D-0530-0037,FDA,FDA-2012-D-0530,EPFP OverviewDocument Template,Supporting & Related Material,Background Material,2022-08-09T04:00:00Z,2022,8,,,2022-08-09T20:33:26Z,,0,0,090000648522a964
FDA-2012-D-0530-0036,FDA,FDA-2012-D-0530,Agency Information Collection Activities; Proposed Collection; Comment Request; Q-Submission Program for Medical Devices,Notice,60 Day Proposed Information Collection,2022-08-09T04:00:00Z,2022,8,2022-08-09T04:00:00Z,2022-10-12T03:59:59Z,2022-12-22T14:51:20Z,2022-17058,0,0,09000064852266f0