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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K930091
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Product Description
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FDA Recall
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CORDIS-SV-5 Steerable Guidewire, 300 cm.,5 Steerable Guidewires,Cordis a Johnson Johnson Company ,EN... 2 09/09/2006 FEI # 1016427
Cordis Corporation
CORDIS SV-8 Steerable Guidewire, 300 cm., 5 Steerable Guidewires, Cordis a Johnson Johnson Company E... 2 09/09/2006 FEI # 1016427
Cordis Corporation
CORDIS SV-8 Steerable Guidewire, 180 cm. , 5 Steerable Guidewires, Cordis a Johnson Johnson Company,... 2 09/09/2006 FEI # 1016427
Cordis Corporation
CORDIS SV-5 Steerable Guidewire, 180 cm., 5 Steerable Guidewires, Cordis a Johnson Johnson Company, ... 2 09/09/2006 FEI # 1016427
Cordis Corporation
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