Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K153402 |
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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 Nuclear Medicine 600/800 series systems, specifically: a) 870 CZT O540+ Gantry 7.25mm, b) D670 ... | 1 | 02/08/2023 |
FEI # 3004571294 GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING |
| GE NM/CT 870 CZT system Model Number H3906CW - Product Usage: intended for general Nuclear Medicine ... | 2 | 01/13/2021 |
FEI # 2126677 GE Healthcare, LLC |
| NM/CT 870 CZT Model # H3906CW | 2 | 09/21/2020 |
FEI # 2126677 GE Healthcare, LLC |
| Discovery NM/CT 670 CZT, Model/Catalogue/Code H3906CT Product Usage: The GE Discovery NM/CT 670 ... | 2 | 05/03/2019 |
FEI # 2126677 GE Healthcare, LLC |
| NM/CT 870 CZT, Model/Catalogue/Code # H3906CW Product Usage: The GE Discovery NM/CT 670 CZT syst... | 2 | 05/03/2019 |
FEI # 2126677 GE Healthcare, LLC |
| GE Healthcare Discovery NM/CT 670 CZT X-ray system | 2 | 06/12/2017 |
FEI # 2126677 GE Healthcare, LLC |
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