FDA 510(k), K170867, FTRD System Set

FDA 510(k), K170867, FTRD System Set

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510(K) Number: K170867
Device Name: FTRD System Set
Manufacturer: Ovesco Endoscopy AG
Device Classification Name: hemostatic metal clip for the gi tract
Regulation Number: 876.4400
Classification Product Code: PKL
Date Received: 03/23/2017
Decision Date: 07/25/2017
Regulation Medical Specialty: Gastroenterology/Urology

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