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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Stapler, Surgical
510(k) Number K862772
Device Name V. MUELLER (R) GOOSENECK CIRCULAR STAPLER
Applicant
American V. Mueller
6600 W. Touhy
Chicago,  IL  60648
Applicant Contact MATTHEW NOWLAND
Correspondent
American V. Mueller
6600 W. Touhy
Chicago,  IL  60648
Correspondent Contact MATTHEW NOWLAND
Regulation Number878.4740
Classification Product Code
GAG  
Date Received07/22/1986
Decision Date 08/18/1986
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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