Medical Device Recalls
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1 result found
510(K) Number: K233650 |
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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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| SOMATOM X.ceed Software applications: syngo.CT Brain Quantification syngo.CT Vessel Hyperdensiti... | 2 | 02/03/2026 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
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