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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 6 of 6 Results
510(K) Number: K933625
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Product Description
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FDA Recall
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ASY Brat 2 Procedure Set, for blood recovery & autotransfusion. 2 08/03/2005 Cobe Cardiovascular, Inc
ASY Brat 2 Procedure Set 2 08/03/2005 Cobe Cardiovascular, Inc
ASY Brat 2 Procedure Set 2 08/03/2005 Cobe Cardiovascular, Inc
ASY, Brat 2 Pack Procedure Set 2 08/03/2005 Cobe Cardiovascular, Inc
ASY, Brat 2 Procedure Set 2 08/03/2005 Cobe Cardiovascular, Inc
ASY, Brat Pack Procedure Set 2 08/03/2005 Cobe Cardiovascular, Inc
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