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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 K920273
Device Name HEMOVAC AUTOTRANSFUSION SYSTEM
Original Applicant
ZIMMER PATIENT CARE DIVISION
200 w. ohio ave.
p.o. box 10
dover,  OH  44622
Original Contact paula s osorio
Regulation Number868.5830
Classification Product Code
CAC  
Date Received01/22/1992
Decision Date 01/28/1993
Decision substantially equivalent (SE)
Classification Advisory Committee Anesthesiology
Review Advisory Committee Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No
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