Medical Device Recalls
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1 result found
510(K) Number: K222116 |
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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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| Atellica CI Analyzer. Catalog Numbers: 10947347. | 2 | 12/04/2024 |
FEI # 2432235 Siemens Healthcare Diagnostics, Inc. |
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