Medical Device Recalls
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1 result found
510(K) Number: K200213 |
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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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| Biograph mMR. Model Number: 10433372. | 1 | 09/30/2025 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
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