documents: FDA-2008-D-0611-0002

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id
FDA-2008-D-0611-0002 FDA FDA-2008-D-0611 Draft Guidance for Industry and FDA Staff - Submission and review of sterility information in premarket notification (510(k)) submissions for devices labeled as sterile - Guidance Other GDL-Guidance (Supporting and Related Materials) 2008-12-12T05:00:00Z 2008 12     2013-07-27T22:33:12Z   0 0 09000064807d88e6

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