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FDA 510(k) K963160, HX-5/6-1 ENDOSCOPIC CLIPPING DEVICE, by Olympus America, Inc.

FDA 510(k) K963160, HX-5/6-1 ENDOSCOPIC CLIPPING DEVICE, by Olympus America, Inc.

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510(K) Number: K963160
Device Name: HX-5/6-1 ENDOSCOPIC CLIPPING DEVICE
Manufacturer: Olympus America, Inc.
Device Classification Name: hemostatic metal clip for the gi tract
Regulation Number: 876.4400
Classification Product Code: PKL
Date Received: 08/14/1996
Decision Date: 06/27/1997
Regulation Medical Specialty: Gastroenterology/Urology
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