Medical Device Recalls
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1 result found
510(K) Number: K812032 |
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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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| MEVATRON M 6730/6740 (MEX) Accelerator, Linear, Medical The intended use of the SIEMENS branded PRI... | 2 | 03/09/2017 | Siemens Medical Solutions USA, Inc |
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