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withdrawn,object_id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-1529-0029,FDA,FDA-2013-N-1529,Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals,Notice,General Notice,2022-04-07T04:00:00Z,2022,4,2022-04-07T04:00:00Z,,2022-04-07T14:27:45Z,2022-07394,0,0,0900006484fff28f
FDA-2013-N-1529-0026,FDA,FDA-2013-N-1529,"Agency Information Collection
Activities; Submission for Office of
Management and Budget Review;
Comment Request; Reclassification
Petitions for Medical Devices",Notice,30 Day Proposed Information Collection,2021-12-29T05:00:00Z,2021,12,2021-12-29T05:00:00Z,2022-01-29T04:59:59Z,2021-12-29T17:25:49Z,2021-28299,0,0,0900006484effa24
FDA-2013-N-1529-0027,FDA,FDA-2013-N-1529,"Agency Information Collection
Activities; Submission for Office of
Management and Budget Review;
Comment Request; Reclassification
Petitions for Medical Devices",Notice,30 Day Proposed Information Collection,2021-12-29T05:00:00Z,2021,12,2021-12-29T05:00:00Z,2022-01-29T04:59:59Z,2022-01-29T02:00:36Z,2021-28305,0,0,0900006484effb4a
FDA-2013-N-1529-0025,FDA,FDA-2013-N-1529,Agency Information Collection Activities; Proposed Collection; Comment Request; Reclassification Petitions for Medical Devices,Notice,60 Day Proposed Information Collection,2021-09-07T04:00:00Z,2021,9,2021-09-07T04:00:00Z,2021-11-09T04:59:59Z,2021-09-07T14:32:55Z,2021-19221,0,0,0900006484d568f2
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
FDA-2013-N-1529-0020,FDA,FDA-2013-N-1529,"Medical Device Classification Procedures: Incorporating Food and
Drug Administration Safety and Innovation Act Procedures",Rule,Final Rule,2018-12-17T05:00:00Z,2018,12,2018-12-17T05:00:00Z,,2018-12-17T14:46:15Z,2018-27015,0,0,090000648399cf84
FDA-2013-N-1529-0019,FDA,FDA-2013-N-1529,Medical Device Classification Procedures; Change of Address; Technical Amendment,Rule,Correction,2017-08-21T04:00:00Z,2017,8,2017-08-21T04:00:00Z,,2017-08-21T15:12:40Z,2017-17564,0,0,0900006482a8b3e2
FDA-2013-N-1529-0018,FDA,FDA-2013-N-1529,Medical Device Classification Procedures: Reclassification Petition: Content and Form; Technical Amendment,Rule,Final Rule,2014-12-24T05:00:00Z,2014,12,,,2014-12-24T17:15:31Z,2014-30141,0,0,090000648199128e
FDA-2013-N-1529-0002,FDA,FDA-2013-N-1529,Medical Device Classification Procedures; Extension of Comment Period,Proposed Rule,Extension of Comment Period,2014-06-12T04:00:00Z,2014,6,2014-06-12T04:00:00Z,2014-09-23T03:59:59Z,2014-12-24T17:10:11Z,2014-13705,0,0,0900006481740c73
FDA-2013-N-1529-0001,FDA,FDA-2013-N-1529,Medical Device Classification Procedures,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2014-03-25T04:00:00Z,2014,3,2014-03-25T04:00:00Z,2014-06-24T03:59:59Z,2014-06-21T01:04:55Z,2014-06364,0,0,090000648167c778