Medical Device Recalls
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1 result found
510(K) Number: K231701 |
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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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| Ziehm Vision RFD 3D. Interventinoal fluoroscopic x-ray system | 2 | 12/02/2024 | Orthoscan, Inc. |
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