documents: FDA-2016-P-0159-0004

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-P-0159-0004 FDA FDA-2016-P-0159 Procedures for Class II Device Exemptions from Premarket Notification, Guidance for Industry and CDRH Staff re Medical Devices; Exemption From Premarket Notification: Method, Metallic Reduction, Glucose (Urinary, Non-Quantitative) Test System in a Reagent Tablet Format Supporting & Related Material Background Material 2016-03-24T04:00:00Z 2016 3     2016-03-28T19:32:37Z   0 0 0900006481edd298

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