documents: FDA-2021-N-0913-0001

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2021-N-0913-0001 FDA FDA-2021-N-0913 Medical Devices; Cardiovascular Devices; Classification of the Photoplethysmograph Analysis Software for Over-the-Counter Use Rule Final Rule 2022-02-04T05:00:00Z 2022 2 2022-02-04T05:00:00Z   2022-02-04T15:45:31Z 2022-02358 0 0 0900006484f54982

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