Medical Device Recalls
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1 to 7 of 7 Results
510(K) Number: K111551 |
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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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Series OEC 9800. The Series OEC 9800 is designed to provide fluoroscopic and spot-film imaging of... | 2 | 11/07/2014 | GE OEC Medical Systems, Inc |
OEC 9800, fluoroscopic x-ray system | 2 | 08/23/2016 | GE OEC Medical Systems, Inc |
OEC 9800. MDL Numbers: D222250, D141598 The OEC 9800 is designed to provide fluoroscopic and spot-f... | 2 | 01/09/2017 | GE OEC Medical Systems, Inc |
OEC 9800. MDL Numbers: D222250, D141598 | 2 | 01/20/2017 | 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 |
OEC 9800 Systems with 9-inch Image Intensifier | 2 | 07/31/2023 | GE OEC Medical Systems, Inc |
Field Upgrade Kits: P/N 5451208 RIU, 9 INCH, TOSHIBA; P/N 5485304 SERVICE PART, IMAGE INTENSIFIER, 9... | 2 | 07/31/2023 | GE OEC Medical Systems, Inc |
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