Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K943805 |
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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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Prestige II, Prestige SI, Prestige VH Prestige system is a new multi-purpose conventional and di... | 2 | 06/10/2019 | GE Healthcare, LLC |
Prestige II | 2 | 12/23/2016 | GE Healthcare, LLC |
Prestige SI | 2 | 12/23/2016 | GE Healthcare, LLC |
Prestige VH | 2 | 12/23/2016 | GE Healthcare, LLC |
Video Monitor Suspensions that may be on the following Fluoroscopic and Radiographic X-Ray systems: ... | 2 | 01/21/2014 | GE Healthcare, LLC |
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