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withdrawn,object_id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-N-0303-0005,FDA,FDA-2012-N-0303,Medical Devices: Gastroenterology-Urology Devices; Implanted Blood Access Devices; Reclassification,Rule,Final Rule,2014-07-25T04:00:00Z,2014,7,2014-07-25T04:00:00Z,,2014-07-28T12:32:21Z,2014-17477,0,0,09000064817e1570
FDA-2012-N-0303-0003,FDA,FDA-2012-N-0303,Gastroenterology-Urology Devices; Reclassification of Implanted Blood Access Devices,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2013-06-28T04:00:00Z,2013,6,2013-06-28T04:00:00Z,2013-07-30T03:59:59Z,2014-01-14T13:32:34Z,2013-15504,0,0,0900006481348988
FDA-2012-N-0303-0002,FDA,FDA-2012-N-0303,Gastroenterology Urology Devices Reclassification of Implanted Blood Access Devices,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2012-06-20T04:00:00Z,2012,6,2012-06-20T04:00:00Z,2012-09-19T03:59:59Z,2013-08-28T01:02:25Z,2012-15024,0,0,090000648105a25e
FDA-2012-N-0303-0001,FDA,FDA-2012-N-0303,Gastroenterology Urology Devices Reclassification of Implanted Blood Access Devices,Proposed Rule,,2012-06-20T00:00:00Z,2012,6,,,2012-06-20T16:11:16Z,,0,1,09000064810594af