Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K082781 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| The OEC 9900 Elite mobile fluoroscopy system (image intensified fluoroscopic x-ray) is designed to p... | 2 | 04/16/2014 | GE OEC Medical Systems, Inc |
| OEC 9900 Systems with 9-inch Image Intensifier | 2 | 07/31/2023 | GE OEC Medical Systems, Inc |
| OEC 9900 REF Image-Intensified Fluoroscopic X-Ray System, Mobile. The OEC 9900 Elite mobile fluo... | 2 | 12/18/2024 | GE OEC Medical Systems, Inc |
| GE HealthCare OEC 9900 Elite C-arm Systems. | 2 | 08/22/2025 | GE Medical Systems, LLC |
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