Medical Device Recalls
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1 result found
510(K) Number: K050857 |
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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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| BIB Balloon in Balloon Dilatation Catheter. Model Number: 420 | 2 | 05/13/2025 |
FEI # 1318694 Numed Inc |
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