Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K091536 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| System, Nuclear Magnetic Resonance Imaging - Product Usage: is a whole body magnetic resonance scann... | 2 | 10/20/2020 |
FEI # 2126677 GE Healthcare, LLC |
| Optima MR450w 1.5T Product Usage: The Optima MR450w 1.5T system is a whole body magnetic resonan... | 2 | 08/02/2017 |
FEI # 2183553 GE Medical Systems, LLC |
| GE Healthcare, Optima MR450w 1.5T MR systems The GE Signa® MR750 System is a whole body magnetic re... | 2 | 02/18/2011 |
FEI # 2126677 GE Healthcare, LLC |
| GE Healthcare, 1.5T Optima MR450w Product Usage: The Optima MR450w is a whole body magnetic res... | 2 | 09/01/2011 |
FEI # 2126677 GE Healthcare, LLC |
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