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withdrawn,object_id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-1439-0003,FDA,FDA-2013-N-1439,"Agency Information Collection Activities; Announcement of Office of
Management and Budget Approval; Adverse Event Program for Medical
Devices (Medical Product Safety Network)",Notice,Notice of Approval,2014-06-18T04:00:00Z,2014,6,2014-06-18T04:00:00Z,,2014-06-18T14:11:11Z,2014-14252,0,0,090000648174fbcc
FDA-2013-N-1439-0002,FDA,FDA-2013-N-1439,"Agency Information Collection Activities; Submission for Office of
Management and Budget Review; Comment Request; Adverse Event
Program for Medical Devices (Medical Product Safety Network)",Notice,General Notice,2014-04-14T04:00:00Z,2014,4,2014-04-14T04:00:00Z,2014-05-15T03:59:59Z,2014-04-14T14:04:23Z,2014-08212,0,0,09000064816b252d
FDA-2013-N-1439-0001,FDA,FDA-2013-N-1439,Agency Information Collection Activities; Proposed Collection; Comment Request; Adverse Event Program for Medical Products,Notice,General Notice,2013-11-29T05:00:00Z,2013,11,2013-11-29T05:00:00Z,2014-01-29T04:59:59Z,2013-11-29T17:16:39Z,2013-28600,0,0,090000648149f214