Medical Device Recalls
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1 result found
510(K) Number: K152665 |
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Product Description
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Recall
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FDA Recall
Posting Date |
Recalling Firm
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| The PolarCath Balloon Catheter consists of a coaxial catheter shaft with two concentric, non-complia... | 2 | 11/21/2019 |
FEI # 3011393614 Nucryo Vascular Inc. |
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