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documents: FDA-2016-P-1026-0004

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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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-P-1026-0004 FDA FDA-2016-P-1026 Reference 1 - Guidance for Industry and CDRH Staff on Procedures for Class II Device Exemptions from Premarket Notification Supporting & Related Material Background Material 2016-06-20T04:00:00Z 2016 6     2024-11-07T23:47:40Z   0 0 090000648204943e

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