Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K033484 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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CryoValve, Pulmonary Valve & Conduit | 2 | 09/01/2008 | CryoLife, Inc. |
CryoValve, Aortic Valve & Conduit | 2 | 09/01/2008 | CryoLife, Inc. |
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