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withdrawn,object_id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-2008-N-0488-0025,FDA,FDA-2008-N-0488,Medical Devices: Ophthalmic Devices; Laser-Assisted In Situ Keratomileusis (LASIK) Devices; Reopening of the Comment Period,Notice,N-Notice,2009-11-13T05:00:00Z,2009,11,2009-11-13T05:00:00Z,2010-11-16T04:59:59Z,2009-11-13T15:03:26Z,E9-27222,0,0,0900006480a56cc2
FDA-2008-N-0488-0001,FDA,FDA-2008-N-0488,Medical Devices: Ophthalmic Devices; Laser-Assisted In Situ Keratomileusis (LASIK) Devices; Establishing a Docket,Notice,N-Notice,2008-09-12T04:00:00Z,2008,9,2008-09-12T04:00:00Z,2009-09-15T03:59:59Z,2008-09-12T12:28:58Z,E8-21339,0,0,09000064807017cb