Medical Device Recalls
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1 result found
510(K) Number: K223439 |
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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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| SIGNA Victor, with affected software versions: MR30.1; Nuclear Magnetic Resonance Imaging System | 2 | 08/02/2024 |
FEI # 2183553 GE Medical Systems, LLC |
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