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withdrawn,object_id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-D-0530-0019,FDA,FDA-2012-D-0530,"Agency Information Collection Activities; Proposals, Submissions, and Approvals: Guidance on Medical Devices; Pre-Submission Program and Meetings with FDA Staff",Notice,30 Day Proposed Information Collection,2012-12-11T05:00:00Z,2012,12,2012-12-11T05:00:00Z,2013-01-11T04:59:59Z,2015-11-12T13:04:02Z,2012-29788,0,0,090000648118589b
FDA-2012-D-0530-0001,FDA,FDA-2012-D-0530,Draft Guidance for Industry and Food and Drug Administration Staff; Medical Devices: The Pre-Submission Program and Meetings With FDA Staff; Availability,Notice,Notice of Availability,2012-07-13T04:00:00Z,2012,7,2012-07-13T04:00:00Z,2012-10-12T03:59:59Z,2012-11-30T21:20:01Z,2012-17078,0,0,09000064810934d0
FDA-2012-D-0530-0002,FDA,FDA-2012-D-0530,Draft Guidance for Industry and Food and Drug Administration Staff Medical Devices The Pre-Submission Program and Meetings with FDA Staff,Other,Guidance,2012-07-13T04:00:00Z,2012,7,2012-07-13T04:00:00Z,2012-10-12T03:59:59Z,2012-10-12T02:02:03Z,,0,0,0900006481094e0c