Medical Device Recalls
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11 to 11 of 11 Results
Recall Date to: 08/04/2015 510(K) Number: K993687 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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OEC Uroview 2800 with Dual Monitor Option, fluoroscopic x-ray system, Model Numbers: 882082-01, 8820... | 2 | 02/15/2007 | GE OEC Medical Systems, Inc |
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