Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K123417 |
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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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| Brivo MR355, NMRI system | 2 | 02/28/2025 |
FEI # 3008284470 GE Healthcare (China) Co., Ltd. |
| Optima MR360, NMRI system | 2 | 02/28/2025 |
FEI # 3008284470 GE Healthcare (China) Co., Ltd. |
| Brivo MR355, Optima MR360 Product Usage: The Brivo MR355/Optima MR360 is a whole body magnetic r... | 2 | 08/02/2017 |
FEI # 2183553 GE Medical Systems, LLC |
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