Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K111242 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| MAGNETOM Aera magnetic resonance diagnostic devices Model # 10432914 | 2 | 08/22/2019 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
| MAGNETOM Skyra magnetic resonance diagnostic devices Model # 10432915 | 2 | 08/22/2019 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
| MAGNETOM Aera magnetic resonance system. Indicated for use as a magnetic resonance diagnostic dev... | 2 | 05/27/2014 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
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