documents: FDA-2013-N-1518-0001
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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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-2013-N-1518-0001 | FDA | FDA-2013-N-1518 | Cardiovascular Devices; Reclassification of Nonroller-Type Cardiopulmonary Bypass Blood Pumps for Cardiopulmonary and Circulatory Bypass; Effective Date of Requirement for Premarket Approval for Nonroller-Type Cardiopulmonary Bypass Blood Pumps for Temporary Ventricular Support | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2014-01-07T05:00:00Z | 2014 | 1 | 2014-01-07T05:00:00Z | 2014-04-08T03:59:59Z | 2014-04-08T01:06:02Z | 2014-00027 | 0 | 0 | 09000064814f1384 |
Links from other tables
- 1 row from regs_document_id in fr_regs_crossref