documents: FDA-2022-N-0794-0001
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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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-2022-N-0794-0001 | FDA | FDA-2022-N-0794 | General and Plastic Surgery Devices; Reclassification of Optical Diagnostic Devices for Melanoma Detection and Electrical Impedance Spectrometers, To Be Renamed Computer-Aided Devices Which Provide Adjunctive Diagnostic Information About Lesions Suspicious for Melanoma | Proposed Rule | Amendment | 2022-06-30T04:00:00Z | 2022 | 6 | 2022-06-30T04:00:00Z | 2022-08-30T03:59:59Z | 2022-08-31T01:01:03Z | 2022-13954 | 0 | 0 | 09000064851ab45e |
Links from other tables
- 1 row from regs_document_id in fr_regs_crossref