Medical Device Recalls
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11 to 11 of 11 Results
Recall Date to: 03/02/2015 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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UroView 2800; MDL number A349855. Product Usage: Designed to provide fluoroscopic and spot-film i... | 2 | 08/01/2012 | GE OEC Medical Systems, Inc |
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