Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K013586 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Magnetom Trio MRI System, Model 7106441 | 2 | 08/24/2004 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
| Magnetom Trio MRI System, Model 7387074 | 2 | 08/24/2004 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
| Magnetom Trio System. Nuclear Magnetic Resonance Imaging Diagnostic Device | 3 | 02/10/2004 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
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