Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K131576 |
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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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| GE Healthcare Optima CT660. The systems are intended for head, whole body, cardiac and vascular X-r... | 2 | 08/17/2018 |
FEI # 3002808529 GE Healthcare Japan Corporation |
| GE Healthcare Revolution EVO X-ray system | 2 | 06/12/2017 |
FEI # 2126677 GE Healthcare, LLC |
| GE Healthcare Revolution EVO, Model Number 5454001-260; X-ray/computed tomography system | 2 | 12/04/2024 |
FEI # 3008284470 GE Healthcare (China) Co., Ltd. |
| GE Healthcare Revolution EVO, Optima CT660, Optima CT670, Optima CT680. The systems are intended fo... | 2 | 08/17/2018 |
FEI # 3002808529 GE Healthcare Japan Corporation |
| Revolution EVO 3.6, labeled as a. HVY WAUK; b. LONG HINO; c. LONG WAUK; d. MID BJG; ... | 2 | 07/31/2018 |
FEI # 2126677 GE Healthcare, LLC |
| Revolution EVO, Optima CT660, Optima CT680 CT Systems. | 2 | 06/25/2021 |
FEI # 2126677 GE Healthcare, LLC |
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