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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Endoscopic Retrograde Cholangiopancreatography (Ercp) Cannula
510(k) Number K820431
FOIA Releasable 510(k) K820431
Device Name E.R.C.P. CANNULAS
Applicant
American Endoscopy, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
American Endoscopy, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number876.1500
Classification Product Code
ODD  
Date Received02/17/1982
Decision Date 04/09/1982
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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