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withdrawn,object_id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-N-0650-0026,FDA,FDA-2011-N-0650,Cardiovascular Devices; Reclassification of External Pacemaker Pulse Generator Devices; Reclassification of Pacing System Analyzers,Rule,Final Rule,2016-04-18T04:00:00Z,2016,4,2016-04-18T04:00:00Z,,2016-04-18T18:52:03Z,2016-08898,0,0,0900006481f70626