Medical Device Recalls
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1 result found
510(K) Number: K052775 |
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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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CT syngo Dual Energy Viewer on the syngo Multimodality Work Place (MMWP) and on the CT workplace, Mo... | 2 | 01/08/2009 | Siemens Medical Solutions USA, Inc |
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