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withdrawn,object_id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-2000-P-0924-0001,FDA,FDA-2000-P-0924,Notice of Panel Recommendation- Cardiovascular Devices; Reclassification of Certain Percutaneous Transluminal Coronary Angioplasty Catheters,Notice,N-Notice,2008-05-30T04:00:00Z,2008,5,2008-05-30T04:00:00Z,2008-08-29T03:59:59Z,2024-08-08T16:29:34Z,E8-12079,0,0,09000064806072d2