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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 K902059
Device Name AUTOWAND(TM) 7XXX SERIES
Original Applicant
BOEHRINGER LABORATORIES
p.o. box 870
norristown,  PA  19404
Original Contact karpowicz, m.e.
Regulation Number868.5830
Classification Product Code
CAC  
Date Received05/07/1990
Decision Date 07/24/1990
Decision substantially equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No
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