Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K132027 |
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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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| Series OEC 9800. The Series OEC 9800 is designed to provide fluoroscopic and spot-film imaging of... | 2 | 11/07/2014 |
FEI # 1720753 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 |
FEI # 1720753 GE OEC Medical Systems, Inc |
| OEC 9800. MDL Numbers: D222250, D141598 | 2 | 01/20/2017 |
FEI # 1720753 GE OEC Medical Systems, Inc |
| GE HealthCare OEC 9800. | 2 | 08/22/2025 |
FEI # 2126677 GE Medical Systems, LLC |
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