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withdrawn,object_id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-D-0476-0010,FDA,FDA-2011-D-0476,Guidance for Industry and Staff; Enforcement Policy for Premarket Notification Requirements for Certain In Vitro Diagnostic and Radiology Devices,Other,Guidance,2011-12-20T05:00:00Z,2011,12,2011-12-20T05:00:00Z,,2020-04-29T14:40:32Z,,0,0,0900006480f8692a
FDA-2011-D-0476-0009,FDA,FDA-2011-D-0476,Guidance for Industry and Staff; Availability: Enforcement Policy for Premarket Notification Requirements for Certain In Vitro Diagnostic and Radiology Devices,Notice,Notice of Availability,2011-12-20T05:00:00Z,2011,12,2011-12-20T05:00:00Z,,2012-03-24T19:36:40Z,2011-32437,0,0,0900006480f86544
FDA-2011-D-0476-0001,FDA,FDA-2011-D-0476,Draft Guidance for Industry and Food and Drug Administration Staff: Enforcement Policy for Premarket Notification Requirements for Certain In Vitro Diagnostic and Radiology Devices,Notice,Notice of Availability,2011-07-12T04:00:00Z,2011,7,2011-07-12T04:00:00Z,2011-10-12T03:59:59Z,2011-10-12T20:38:43Z,2011-17352,0,0,0900006480ec0678