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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Staple, Removable (Skin)
510(k) Number K851974
Device Name V. MUELLER VITAL SKIN STAPLER
Applicant
American V. Mueller
6600 W. Touhy
Chicago,  IL  60648
Applicant Contact MATHEW NOWLAND
Correspondent
American V. Mueller
6600 W. Touhy
Chicago,  IL  60648
Correspondent Contact MATHEW NOWLAND
Regulation Number878.4760
Classification Product Code
GDT  
Date Received05/07/1985
Decision Date 06/11/1985
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
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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