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documents: FDA-2017-P-5124-0005

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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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2017-P-5124-0005 FDA FDA-2017-P-5124 Medical Devices: Exemption from Premarket Notification; Class II Devices; Over-the-Counter Denture Repair Kit Rule Final Rule 2018-03-14T04:00:00Z 2018 3 2018-03-14T04:00:00Z   2018-03-14T14:20:53Z 2018-05116 0 0 090000648300e7c9

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