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withdrawn,object_id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-2026-N-0232-0001,FDA,FDA-2026-N-0232,Medical Devices; Exemptions From Premarket Notification: Class II Devices; Request for Comments,Notice,Request for Comments,2026-02-06T05:00:00Z,2026,2,2026-02-06T05:00:00Z,2026-04-08T03:59:59Z,2026-02-26T10:00:18Z,2026-02377,1,0,09000064b9195af7
FDA-2026-N-0232-0002,FDA,FDA-2026-N-0232,Reference 1 - Procedures for Class II Device Exemptions from Premarket Notification Guidance for Industry and CDRH Staff,Supporting & Related Material,Background Material,2026-02-06T05:00:00Z,2026,2,,,2026-02-06T20:51:33Z,,0,0,09000064b9196169