documents: FDA-2009-N-0114-0002

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

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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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2009-N-0114-0002 FDA FDA-2009-N-0114 OMB Review, EO12866, Regulatory Policy and Management Staff Note to the Division of Dockets Management, May 5, 2010 - [Implementation of Device Registration and Listing Requirements Enacted in Section 321 of the Public Health Security and Bioterrorism Preparedness and Response Act of 2002, and Title II of the FDAAA 2007; Proposed Rule, March 26, 2010] - Reference Other REF-Reference 2010-05-18T04:00:00Z 2010 5 2010-05-18T04:00:00Z   2013-07-27T23:18:10Z   0 0 0900006480ae7f91

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