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Regulatory documents from Regulations.gov including rules, proposed rules, notices, and supporting materials.

Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API

13 rows where docket_id = "FDA-2013-N-1529" sorted by posted_date descending

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posted_year 6

document_type 4

agency_id 1

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posted_date ▲ posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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

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CREATE TABLE documents (
    id TEXT PRIMARY KEY,
    agency_id TEXT,
    docket_id TEXT REFERENCES dockets(id),
    title TEXT,
    document_type TEXT,
    subtype TEXT,
    posted_date TEXT,
    posted_year INTEGER,
    posted_month INTEGER,
    comment_start_date TEXT,
    comment_end_date TEXT,
    last_modified TEXT,
    fr_doc_num TEXT,
    open_for_comment INTEGER,
    withdrawn INTEGER,
    object_id TEXT
);
CREATE INDEX idx_docs_agency ON documents(agency_id);
CREATE INDEX idx_docs_docket ON documents(docket_id);
CREATE INDEX idx_docs_date ON documents(posted_date);
CREATE INDEX idx_docs_year ON documents(posted_year);
CREATE INDEX idx_docs_type ON documents(document_type);
CREATE INDEX idx_docs_frnum ON documents(fr_doc_num);
CREATE INDEX idx_docs_comment_end ON documents(comment_end_date) WHERE comment_end_date IS NOT NULL AND withdrawn = 0;