documents: FDA-2016-N-0406-0006

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2016-N-0406-0006 FDA FDA-2016-N-0406 Reference 4 - Guidance for Industry and FDA Staff - Guidance for the Content of Premarket Submissions for Software Contained in Medical Devices re Medical Devices; Hematology and Pathology Devices; Classification of Blood Establishment Computer Software and Accessories Supporting & Related Material Background Material 2016-03-01T05:00:00Z 2016 3     2016-03-03T17:13:53Z   0 0 0900006481e9506e

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