Medical Device Recalls
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1 result found
510(K) Number: K223560 |
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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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| Plato 17 Microcatheter REF PL17-160-090 To assist in delivery of therapeutic devices and emboliza... | 2 | 02/26/2025 |
FEI # 3009546466 Scientia Vascular, Inc. |
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