510(k) K963051

ERCP CANNULA by United States Endoscopy Group, Inc. — Product Code ODD

K963051 is an FDA 510(k) premarket notification submitted by United States Endoscopy Group, Inc. for the device "ERCP CANNULA". The FDA issued a decision of Substantially Equivalent on March 28, 1997. The device falls under product code ODD (Endoscopic Retrograde Cholangiopancreatography (Ercp) Cannula), a Class II device regulated under 21 CFR 876.1500. United States Endoscopy Group, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 28, 1997
Date Received
August 6, 1996
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Endoscopic Retrograde Cholangiopancreatography (Ercp) Cannula
Device Class
Class II
Regulation Number
876.1500
Review Panel
GU
Submission Type

To identify stones, tumors, or narrowing in the biliary tree.