documents: FDA-1992-S-0039-0060

Regulatory documents from Regulations.gov including rules, proposed rules, notices, and supporting materials.

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-1992-S-0039-0060 FDA FDA-1992-S-0039 FDA/CDRH Memo to the Division of Dockets Management Submission of Device Information (DI) record to the Global Unique Device Identification Database (GUDID), in compliance with the Unique Device Identification Rule - Memorandum Supporting & Related Material Background Material 2013-12-02T05:00:00Z 2013 12     2013-12-02T21:29:02Z   0 0 09000064814a18df

Links from other tables