FDA 510(k), K953967, ENDOSCOPIC CATHETER

FDA 510(k), K953967, ENDOSCOPIC CATHETER

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510(K) Number: K953967
Device Name: ENDOSCOPIC CATHETER
Manufacturer:
Device Classification Name: Endoscopic Retrograde Cholangiopancreatography (Ercp) Cannula
Regulation Number: 876.1500
Classification Product Code: ODD
Date Received: 08/22/1995
Decision Date: 01/22/1996
Regulation Medical Specialty: Gastroenterology/Urology
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