Medical Device Recalls
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1 result found
510(K) Number: K061953 |
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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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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 |
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