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withdrawn,object_id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-0650-0001,FDA,FDA-2011-N-0650,Cardiovascular Devices: Reclassification of External Pacemaker Pulse Generator Devices,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2011-10-17T04:00:00Z,2011,10,2011-10-17T04:00:00Z,2012-01-18T04:59:59Z,2011-10-17T13:19:24Z,2011-26625,0,0,0900006480f54001