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withdrawn,object_id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-2013-N-1529-0021,FDA,FDA-2013-N-1529,"01 Index to References - Final Rule, Medical Device Classification Procedures: Incorporating FDA Safety and Innovation Act Procedures",Other,Reference Materials,2019-02-25T05:00:00Z,2019,2,2019-02-25T05:00:00Z,,2019-02-25T19:12:12Z,,0,0,0900006483aa4e5d
FDA-2013-N-1529-0023,FDA,FDA-2013-N-1529,"03 Reference 2 Open Public Hearings Guidance - Guidance for the Public, FDA Advisory Committee Members, and FDA Staff: The Open Public Hearing at FDA Advisory Committee Meetings",Other,Guidance,2019-02-25T05:00:00Z,2019,2,2019-02-25T05:00:00Z,,2019-02-25T19:15:36Z,,0,0,0900006483aa4b3c
FDA-2013-N-1529-0024,FDA,FDA-2013-N-1529,04 Reference 3 Final Regulatory Impact Analysis - Medical Device Classification Procedures: Incorporating FDA Safety and Innovation Act Procedures,Other,Reference Materials,2019-02-25T05:00:00Z,2019,2,2019-02-25T05:00:00Z,,2019-02-25T19:19:01Z,,0,0,0900006483aa4b3e
FDA-2013-N-1529-0022,FDA,FDA-2013-N-1529,02 Reference 1 Medical Device Classification Product Codes Guidance for Industry,Other,Guidance,2019-02-25T05:00:00Z,2019,2,2019-02-25T05:00:00Z,,2019-02-25T19:11:36Z,,0,0,0900006483aa4b38