documents
Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API
7 rows where docket_id = "FDA-2018-D-4115" sorted by posted_date descending
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Suggested facets: subtype, posted_date, posted_month, comment_start_date, last_modified, open_for_comment, posted_date (date), comment_start_date (date), comment_end_date (date), last_modified (date)
| 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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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-2018-D-4115-0019 | FDA | None FDA-2018-D-4115 | Clarification of Radiation Control Regulations for Manufacturers of Diagnostic X-Ray Equipment; Guidance for Industry and Food and Drug Administration Staff; Availability | Notice | Notice of Availability | 2024-09-30T04:00:00Z | 2024 | 9 | 2024-09-30T14:16:58Z | 2024-22332 | 0 | 0 | 09000064867a0335 | ||
| FDA-2018-D-4115-0020 | FDA | None FDA-2018-D-4115 | Clarification of Radiation Control Regulations For Manufacturers of Diagnostic X-Ray Equipment; Guidance for Industry and Food and Drug Administration Staff; Final Guidance | Other | Guidance | 2024-09-30T04:00:00Z | 2024 | 9 | 2024-09-30T04:00:00Z | 2024-11-12T22:47:39Z | 1 | 0 | 09000064867a117d | ||
| FDA-2018-D-4115-0018 | FDA | None FDA-2018-D-4115 | Assembler’s Guide to Diagnostic X-Ray Equipment Guidance for Industry and Food and Drug Administration Staff | Other | Guidance | 2023-02-21T05:00:00Z | 2023 | 2 | 2023-02-21T05:00:00Z | 2024-11-07T00:47:13Z | 1 | 0 | 09000064856e1544 | ||
| FDA-2018-D-4115-0001 | FDA | None FDA-2018-D-4115 | Clarification of Radiation Control Regulations for Manufacturers of Diagnostic X-Ray Equipment; Draft Guidance for Industry and Food and Drug Administration Staff; Availability | Notice | Notice of Availability | 2018-12-17T05:00:00Z | 2018 | 12 | 2018-12-17T05:00:00Z | 2019-02-16T04:59:59Z | 2024-11-12T22:52:39Z | 2018-27236 | 1 | 0 | 090000648399cd0c |
| FDA-2018-D-4115-0002 | FDA | None FDA-2018-D-4115 | Draft Guidance for Industry and FDA_Clarification of Radiation Control Regulations for Diagnostic X-Ray Equipment_issued December 17 2018 | Other | Guidance | 2018-12-17T05:00:00Z | 2018 | 12 | 2018-12-17T05:00:00Z | 2019-02-16T04:59:59Z | 2024-09-30T21:03:13Z | 0 | 0 | 090000648399d6ea | |
| FDA-2018-D-4115-0012 | FDA | None FDA-2018-D-4115 | Guidance for Industry and Food and Drug Administration Staff; Assembler’s Guide to Diagnostic X-Ray Equipment | Other | Guidance | 2011-05-16T04:00:00Z | 2011 | 5 | 2011-05-16T04:00:00Z | 2024-11-06T23:36:50Z | 1 | 0 | 0900006484644a3d | ||
| FDA-2018-D-4115-0013 | FDA | None FDA-2018-D-4115 | The Mammography Quality Standards Act Final Regulations: Preparing For MQSA Inspections; Final Guidance for Industry and FDA | Other | Guidance | 2001-11-04T05:00:00Z | 2001 | 11 | 2001-11-04T05:00:00Z | 2024-11-06T23:36:50Z | 1 | 0 | 0900006484644a3f |
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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;