Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K121072 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Siemens SOMATOM Definition Flash; Intended to produce cross-sectional images of the body. Computed ... | 2 | 04/19/2016 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
| SOMATOM Definition Flash, Computed tomography system Product Usage: SOMATOM Definition AS system... | 2 | 11/17/2016 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
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