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withdrawn,object_id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-2013-N-0487-0004,FDA,FDA-2013-N-0487,"Cardiovascular Devices; Reclassification of External Counter-
Pulsating Devices for Treatment of Chronic Stable Angina; Effective Date
of Requirement for Premarket Approval for External Counter-
Pulsating Devices for Other Specified Intended Uses",Rule,Final Rule,2013-12-30T05:00:00Z,2013,12,2013-12-30T05:00:00Z,,2013-12-30T14:58:02Z,2013-31216,0,0,09000064814e1adf
FDA-2013-N-0487-0001,FDA,FDA-2013-N-0487,Cardiovascular Devices; Reclassification of External Counter-Pulsating Devices for Treatment of Chronic Stable Angina; Effective Date of Requirement for Premarket Approval for External Counter-Pulsating Devices for Other Specified Intended Uses,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2013-05-21T04:00:00Z,2013,5,2013-05-21T04:00:00Z,2013-08-20T03:59:59Z,2014-01-14T13:41:03Z,2013-12122,0,0,09000064812efb10