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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K891576
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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 FEI # 1713910
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 FEI # 1713910
Edwards Lifesciences Research Medical, Inc.
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