Medical Device Recalls
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1 result found
510(K) Number: K203504 |
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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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***Updated 12/4/23*** (1) Cios Flow (VA30) mobile fluoroscopic C-arm X-ray System. Designed for the ... | 2 | 10/27/2023 | Siemens Medical Solutions USA, Inc |
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