Medical Device Recalls
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11 to 12 of 12 Results
510(K) Number: K021049 |
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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| OEC 9800 Plus Fluoroscopic X-ray System, | 2 | 03/22/2007 |
FEI # 1720753 GE OEC Medical Systems, Inc |
| OEC 9800MD Motorized C-arm System, Fluoroscopic X-ray System, | 2 | 03/22/2007 |
FEI # 1720753 GE OEC Medical Systems, Inc |
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