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withdrawn,object_id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-2009-N-0664-0136,FDA,FDA-2009-N-0664,Cardiovascular and Renal Drugs Advisory Committee; Notice of Meeting,Notice,NM-Notice of Meeting,2010-01-11T05:00:00Z,2010,1,,,2010-01-20T04:11:31Z,2010-00173,0,0,0900006480a7b2e4
FDA-2009-N-0664-0135,FDA,FDA-2009-N-0664,The General Hospital and Personal Use Devices Panel of the Medical Devices Advisory Committee; Notice of Meeting,Notice,NM-Notice of Meeting,2010-01-11T05:00:00Z,2010,1,,,2010-01-20T04:11:31Z,2010-00174,0,0,0900006480a7b2a5
FDA-2009-N-0664-0134,FDA,FDA-2009-N-0664,Anesthetic and Life Support Drugs Advisory Committee; Cancellation,Notice,N-Notice,2010-01-06T05:00:00Z,2010,1,,,2010-01-06T12:57:43Z,E9-31306,0,0,0900006480a7791a
FDA-2009-N-0664-0133,FDA,FDA-2009-N-0664,Public Workshop: Medical Device Quality System Regulation Educational Forum on Risk Management Through the Product Life Cycle,Notice,NM-Notice of Meeting,2010-01-05T05:00:00Z,2010,1,,,2010-01-05T14:05:54Z,E9-31198,0,0,0900006480a76f8b