Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K151749 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| SOMATOM Scope, Computed tomography x-ray system | 2 | 06/21/2017 | Siemens Medical Solutions USA, Inc |
| SOMATOM Scope Power, Computed tomography x-ray system | 2 | 06/21/2017 | Siemens Medical Solutions USA, Inc |
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