documents: FDA-2008-N-0571-0001

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2008-N-0571-0001 FDA FDA-2008-N-0571 Agency Information Collection Activities; Proposed Collection; Comment Request; Guidance for Industry and Food and Drug Administration Staff; Compliance With the Medical Device User Fee and Modernization Act of 2002, as Amended: Prominent and Conspicous Mark of Manufacturers on Single-Use Devices (formerly "Reprocessed Single-Use Device Labeling") Notice N-Notice 2008-11-18T05:00:00Z 2008 11 2008-11-18T05:00:00Z 2009-01-17T04:59:59Z 2024-11-12T04:25:39Z   1 0 09000064807b0083

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