documents: FDA-2011-N-0650-0006
Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API
This data as json
| 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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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-2011-N-0650-0006 | FDA | FDA-2011-N-0650 | Cardiovascular Devices; Reclassification of External Pacemaker Pulse Generator Devices; Reclassification of Pacing System Analyzers | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2014-09-15T04:00:00Z | 2014 | 9 | 2014-09-15T04:00:00Z | 2014-12-16T04:59:59Z | 2014-12-16T03:01:20Z | 2014-21814 | 0 | 0 | 0900006481871aee |
Links from other tables
- 1 row from regs_document_id in fr_regs_crossref