Medical Device Recalls
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1 result found
510(K) Number: K203443 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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MR MAGNETOM Systems with RT Image Suite with syngo MR VA20A, VA30A and VA31A with license SW-Key C... | 2 | 09/10/2021 | Siemens Medical Solutions USA, Inc |
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