documents: FDA-2008-D-0611-0017

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-0611-0017 FDA FDA-2008-D-0611 Submission and Review of Sterility Information in Premarket Notification (510(k)) Submissions for Devices Labeled as Sterile: Guidance for Industry and Food and Drug Administration Staff Other Guidance 2016-01-21T05:00:00Z 2016 1 2016-01-21T05:00:00Z   2024-01-08T18:28:21Z   0 0 0900006481e2752a

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