FDA 510(k), K200684, gastroduodenal FTRD Set

FDA 510(k), K200684, gastroduodenal FTRD Set

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510(K) Number: K200684
Device Name: gastroduodenal FTRD Set
Manufacturer: Marc O. Schurr
Device Classification Name: Hemostatic Metal Clip For The Gi Tract
Regulation Number: PKL
Classification Product Code: 03/16/2020
Date Received: 06/02/2020
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Gastroenterology/Urology

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