documents: FDA-2014-N-1210-0001
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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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-2014-N-1210-0001 | FDA | FDA-2014-N-1210 | Neurological Devices; Reclassification of Electroconvulsive Therapy Devices Intended for Use in Treating Severe Major Depressive Episode in Patients 18 Years of Age and Older Who Are Treatment Resistant or Require a Rapid Response; Effective Date of Requirement for Premarket Approval for Electroconvulsive Therapy for Certain Specified Intended Uses | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2015-12-29T05:00:00Z | 2015 | 12 | 2015-12-29T05:00:00Z | 2016-03-29T03:59:59Z | 2019-01-14T20:50:27Z | 2015-32592 | 0 | 0 | 0900006481dd79bf |
Links from other tables
- 1 row from regs_document_id in fr_regs_crossref