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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name apparatus, autotransfusion
510(k) Number K904164
Device Name AUTOVAC (R) AUTOTRANSFUSION SYSTEM, 7900 MODIFIED
Original Applicant
BOEHRINGER LABORATORIES
p.o. box 870
norristown,  PA  19404
Original Contact john karpowicz
Regulation Number868.5830
Classification Product Code
CAC  
Date Received09/11/1990
Decision Date 09/06/1991
Decision substantially equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
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