FDA 510(k), K963160, HX-5/6-1 ENDOSCOPIC CLIPPING DEVICE
FDA 510(k), K963160, HX-5/6-1 ENDOSCOPIC CLIPPING DEVICE
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$149.00 USD
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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
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