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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K033484
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Recall
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FDA Recall
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CryoValve, Aortic Valve & Conduit 2 09/01/2008 FEI # 3001451326
CryoLife, Inc.
CryoValve, Pulmonary Valve & Conduit 2 09/01/2008 FEI # 3001451326
CryoLife, Inc.
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