Medical Device Recalls
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11 to 14 of 14 Results
510(K) Number: K024012 |
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 OEC 9900 Elite Fluoroscopic X-Ray System, GE Healthcare, Surgery, Salt Lake City, Utah. The inte... | 2 | 09/25/2008 |
FEI # 1720753 OEC Medical Systems, Inc |
| OEC 9800, OEC FluoroTrak 9800 Plus, OEC 9800 Plus, OEC 9800 MD Motorized C-arm System designed to pr... | 2 | 07/18/2012 |
FEI # 1720753 GE OEC Medical Systems, Inc |
| OEC 9800; OEC FluoroTrak 9800 Plus; OEC 9800 Plus; OEC 9800 MD Motorized C-arm System, 892.1650 Imag... | 1 | 07/24/2012 |
FEI # 1720753 GE OEC Medical Systems, Inc |
| 892.1650 Image-intensified fluoroscopic x-ray system; the device is designed to provide fluoroscopic... | 2 | 08/22/2012 |
FEI # 1720753 GE OEC Medical Systems, Inc |
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