Medical Device Recalls
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1 result found
510(K) Number: K073472 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| BARD PERIPHERAL VASCULAR VACCESS® PTA Balloon Dilatation Catheters, 8mm x 4cm x 80cm. Product Usa... | 2 | 06/12/2013 |
FEI # 2020394 Bard Peripheral Vascular Inc |
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