Medical Device Recalls
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11 to 11 of 11 Results
Recall Date to: 12/22/2014 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. The UroView 2800 is designed to provide fluoroscopic and spot-film imaging of ... | 2 | 11/07/2014 | GE OEC Medical Systems, Inc |
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