Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K891576 |
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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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Edwards Lifesciences LLC, Fem-Flex II Duraflo Treated Femoral Venous Catheter, 8 Fr. x 11.5 cm, REF ... | 2 | 09/11/2008 | Edwards Lifesciences Research Medical, Inc. |
Edwards Lifesciences LLC, Fem-Flex II Femoral Venous Cannula, 12 Fr. x 11.5 cm, REF FEMII012V, Cardi... | 2 | 09/11/2008 | Edwards Lifesciences Research Medical, Inc. |
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