Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K121160 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| MAGNETOM Spectra as the following: 1. MAGNETOM Spectra. Model Number: 10837643. 2. MAGNETOM Spect... | 1 | 09/30/2025 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
| MAGNETOM Spectra magnetic resonance diagnostic devices Model # 10837643 | 2 | 08/22/2019 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
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