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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Apparatus, Suction, Single Patient Use, Portable, Nonpowered
510(k) Number K873332
Device Name MAXIVAC(TM) CLOSED WOUND SUCTION DRAINAGE SYSTEM
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 Number878.4680
Classification Product Code
GCY  
Date Received08/19/1987
Decision Date 09/08/1987
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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