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withdrawn,object_id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-2002-N-0275-0003,FDA,FDA-2002-N-0275,Agency Information Collection Activities; Announcement of OMB Approval; Medical Device Recall Authority,Notice,Notice of Approval,2003-02-03T05:00:00Z,2003,2,2003-02-04T05:00:00Z,,2025-05-13T02:30:22Z,03-2600,0,0,090000648049e498
FDA-2002-N-0275-0002,FDA,FDA-2002-N-0275,"Agency Information Collection Activities; Submission for OMB Review; Comment Request; Medical
Device Recall Authority",Notice,General Notice,2002-11-13T05:00:00Z,2002,11,2002-11-13T05:00:00Z,2002-12-14T04:59:59Z,2025-05-13T02:28:19Z,02-28713,0,0,090000648049e491
FDA-2002-N-0275-0001,FDA,FDA-2002-N-0275,"Agency Information Collection Activities; Proposed Collection; Comment Request; Medical Device
Recall Authority",Notice,General Notice,2002-08-20T04:00:00Z,2002,8,2002-08-19T04:00:00Z,2002-10-19T03:59:59Z,2025-05-09T20:07:04Z,02-20916,0,0,090000648049e450