Medical Device Recalls
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1 result found
510(K) Number: K232910 |
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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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| CombiDiagnost R90; Model Number: 709031; | 2 | 11/07/2025 | Philips Medical Systems DMC GmbH |
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