Medical Device Recalls
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1 result found
510(K) Number: K202543 |
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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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| Philips OmniWire Pressure guide wire REF 89185J PN 300000252891 | 2 | 06/16/2022 |
FEI # 3008363989 Volcano Corp |
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