documents
Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API
8 rows where docket_id = "FDA-2016-N-0406" and posted_year = 2018 sorted by posted_date descending
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Suggested facets: subtype, last_modified, posted_date (date), comment_start_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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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-2016-N-0406-0018 | FDA | None FDA-2016-N-0406 | Reference 3 - FDA Executive Summary Blood Products Advisory Committee Meeting - December 3 2014 | Supporting & Related Material | Background Material | 2018-05-18T04:00:00Z | 2018 | 5 | 2018-05-18T16:37:43Z | 0 | 0 | 090000648326b5ce | |||
| FDA-2016-N-0406-0015 | FDA | None FDA-2016-N-0406 | Reference 6 - Deciding When to Submit a 510k for a Software Change to an Existing Device Guidance for Industry | Supporting & Related Material | Background Material | 2018-05-18T04:00:00Z | 2018 | 5 | 2018-05-18T16:37:40Z | 0 | 0 | 090000648326b5d1 | |||
| FDA-2016-N-0406-0016 | FDA | None FDA-2016-N-0406 | Reference 5 - Guidance for Industry and FDA Staff - Guidance for the Content of Premarket Submissions for Software Contained in Medical Devices | Supporting & Related Material | Background Material | 2018-05-18T04:00:00Z | 2018 | 5 | 2018-05-18T16:37:42Z | 0 | 0 | 090000648326b5d0 | |||
| FDA-2016-N-0406-0020 | FDA | None FDA-2016-N-0406 | Reference 1 - Blood Products Advisory Committee Meeting transcript-March 20 1998 | Supporting & Related Material | Background Material | 2018-05-18T04:00:00Z | 2018 | 5 | 2018-05-18T16:37:44Z | 0 | 0 | 090000648326b5cc | |||
| FDA-2016-N-0406-0014 | FDA | None FDA-2016-N-0406 | Medical Devices: Hematology and Pathology Devices; Classification of Blood Establishment Computer Software and Accessories | Rule | Final Rule | 2018-05-18T04:00:00Z | 2018 | 5 | 2018-05-18T04:00:00Z | 2018-05-18T14:29:12Z | 2018-10610 | 0 | 0 | 090000648327d5df | |
| FDA-2016-N-0406-0019 | FDA | None FDA-2016-N-0406 | Reference 2 - Blood Products Advisory Committee Meeting transcript - December 3 2014 | Supporting & Related Material | Background Material | 2018-05-18T04:00:00Z | 2018 | 5 | 2018-05-18T16:37:43Z | 0 | 0 | 090000648326b5cd | |||
| FDA-2016-N-0406-0017 | FDA | None FDA-2016-N-0406 | Reference 4 - General Principles of Software Validation Final Guidance for Industry and FDA Staff | Supporting & Related Material | Background Material | 2018-05-18T04:00:00Z | 2018 | 5 | 2018-05-18T16:37:42Z | 0 | 0 | 090000648326b5cf | |||
| FDA-2016-N-0406-0021 | FDA | None FDA-2016-N-0406 | List of References Final Rule | Supporting & Related Material | Background Material | 2018-05-18T04:00:00Z | 2018 | 5 | 2018-05-18T16:37:45Z | 0 | 0 | 090000648326b5cb |
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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;