documents: FDA-2013-N-0581-0001
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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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-0581-0001 | FDA | FDA-2013-N-0581 | Cardiovascular Devices; Reclassification of Intra-Aortic Balloon and Control Systems (IABP) for Acute Coronary Syndrome, Cardiac and Non-Cardiac Surgery, or Complications of Heart Failure; Effective Date of Requirement for Premarket Approval for IABP for Other Specific Intended Uses | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2013-06-19T04:00:00Z | 2013 | 6 | 2013-06-19T04:00:00Z | 2013-09-18T03:59:59Z | 2014-01-14T13:53:46Z | 2013-14553 | 0 | 0 | 0900006481331179 |
Links from other tables
- 1 row from regs_document_id in fr_regs_crossref