documents: FDA-2009-N-0114-0008

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

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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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-0114-0008 FDA FDA-2009-N-0114 Implementation of Device Registration and Listing Requirements Enacted in the Public Health Security and Bioterrorism Preparedness and Response Act of 2002, the Medical Device User Fee and Modernization Act of 2002, and Title II of the Food and Drug Administration Amendments Act of 2007 Rule Final Rule 2012-08-02T04:00:00Z 2012 8     2012-08-02T14:34:56Z 2012-18764 0 0 09000064810beded

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