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documents: FDA-2013-N-0195-0001

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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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2013-N-0195-0001 FDA FDA-2013-N-0195 Effective Date of Requirement for Premarket Approval for Three Class III Preamendments Devices: Reclassification of Sorbent Hemoperfusion Devices for the Treatment of Poisoning and Drug Overdose Proposed Rule Notice of Proposed Rulemaking (NPRM) 2013-04-04T04:00:00Z 2013 4 2013-04-04T04:00:00Z 2013-05-07T03:59:59Z 2014-05-07T01:03:54Z 2013-07730 0 0 0900006481268b15

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