Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K122234 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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OEC 9900 Systems with 9-inch Image Intensifier | 2 | 07/31/2023 | GE OEC Medical Systems, Inc |
OEC 9900 Elite. MDL Numbers: D148942, D155043 | 2 | 01/20/2017 | GE OEC Medical Systems, Inc |
The OEC 9900 Elite mobile fluoroscopy system is designed to provide fluoroscopic and spot-film image... | 2 | 01/09/2017 | GE OEC Medical Systems, Inc |
The OEC 9900 C-Arm is designed to provide fluoroscopic and spot-film images of the patient during di... | 2 | 08/27/2020 | Ge Healthcare |
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