Medical Device Recalls
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1 result found
510(K) Number: K063632 |
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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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| X-Force Nephrostomy Balloon Dilation Catheter Kit with Inflation Device, PTFE Sheath, 8 mm x 15 cm, ... | 2 | 11/04/2016 |
FEI # 1018233 C.R. Bard, Inc. |
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