documents: FDA-2014-D-1318-0002

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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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id
FDA-2014-D-1318-0002 FDA FDA-2014-D-1318 Electroconvulsive Therapy (ECT) Devices for Class II Intended Uses Draft Guidance for Industry, Clinicians and Food and Drug Administration Staff Other Guidance 2015-12-29T05:00:00Z 2015 12 2015-12-29T05:00:00Z   2024-11-11T21:19:55Z   1 0 0900006481dd91f1

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