documents: FDA-2013-N-0195-0001
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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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-0195-0001 | FDA | FDA-2013-N-0195 | Effective Date of Requirement for Premarket Approval for Three Class III Preamendments Devices: Reclassification of Sorbent Hemoperfusion Devices for the Treatment of Poisoning and Drug Overdose | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2013-04-04T04:00:00Z | 2013 | 4 | 2013-04-04T04:00:00Z | 2013-05-07T03:59:59Z | 2014-05-07T01:03:54Z | 2013-07730 | 0 | 0 | 0900006481268b15 |
Links from other tables
- 1 row from regs_document_id in fr_regs_crossref