Medical Device Recalls
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1 result found
510(K) Number: K020693 |
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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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EMBOL-X Slim Access Device / Aortic Cannula 24 Fr X 11''. | 2 | 12/15/2004 | Edwards Lifesciences Research Medical Inc |
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