Medical Device Recalls
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1 result found
510(K) Number: K133174 |
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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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| Mobile Mini C-arm system Part # 1000-0004-FD. Intended to provide the physician with general fluo... | 2 | 01/09/2018 | Orthoscan, Inc. |
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