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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 K952224
Device Name STRYKER CONSTAVAC BLOOD CONSERVATION SYSTEM II (CBCII)
Original Applicant
STRYKER INSTRUMENTS
4100 east milham ave.
kalamazoo,  MI  49001
Original Contact tammy lounds
Regulation Number868.5830
Classification Product Code
CAC  
Date Received05/12/1995
Decision Date 11/17/1995
Decision substantially equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
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