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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 4 of 4 Results
510(K) Number: K030420
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Product Description
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FDA Recall
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Lightspeed 16 CT 2 09/21/2015 GE Healthcare
LightSpeed QX/I (4-slice MDAS) LightSpeed 4.0 CT Scanner System - The LightSpeed 4.0 CT Scanner S... 2 03/04/2016 GE Medical Systems, LLC
GE, VCT for Discovery VCT, Discovery RX VCT, and Discovery PET/CT 690, Lightspeed VCT, Discovery CT7... 2 04/29/2013 GE Healthcare, LLC
GE LightSpeed Pro 16 (100kW/80kW) Models 2357739, 2357739-3, 2357739-4, 2357739-6, 2357739-7 and 235... 2 05/15/2007 GE Healthcare
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