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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
Recall Date to: 11/28/2015 510(K) Number: K040372
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Product Description
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FDA Recall
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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 VCT Select / LightSpeed Pro32, Model 5126093, CT Scanner system. 2 05/15/2007 GE Healthcare
GE LightSpeed VCT / Light Speed VCT standard configuration, Model 5124069, CT Scanner System. 2 05/15/2007 GE Healthcare
The LightSpeed VCT System is intended for head and whole body X-ray Computed Tomography applications... 2 02/15/2007 GE Healthcare
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