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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K943805
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Prestige II 2 12/23/2016 GE Healthcare, LLC
Prestige II, Prestige SI, Prestige VH Prestige system is a new multi-purpose conventional and di... 2 06/10/2019 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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