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withdrawn,object_id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-N-0158-0002,FDA,FDA-2000-N-0158,Medical Devices; Reclassification of the lontophoresis Device,Notice,Notice of Intent,2004-11-04T05:00:00Z,2004,11,2004-11-04T05:00:00Z,2005-02-03T04:59:59Z,2025-06-11T23:54:22Z,04-24591,0,0,09000064804d178a
FDA-2000-N-0158-0003,FDA,FDA-2000-N-0158,Medical Devices; Revision of the Identification of the lontophoresis Device; Withdrawal,Notice,Withdrawal,2004-11-04T05:00:00Z,2004,11,2004-11-04T05:00:00Z,,2025-06-11T23:55:13Z,04-24590,0,0,09000064804d178b