Medical Device Recalls
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1 result found
510(K) Number: K173618 |
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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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| ACUSON AcuNav Volume Intracardiac Echocardiography Catheter 12.5F | 2 | 10/08/2020 | Siemens Medical Solutions USA, Inc. |
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