documents: FDA-2022-N-2375-0003

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2022-N-2375-0003 FDA FDA-2022-N-2375 Authorization of Emergency Use of an In Vitro Diagnostic Device in Response to an Outbreak of Mpox; Availability Notice Announcement 2022-12-30T05:00:00Z 2022 12 2022-12-30T05:00:00Z   2022-12-30T16:46:00Z 2022-28460 0 0 0900006485564bf9

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