Medical Device Recalls
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1 to 4 of 4 Results
Recall Date to: 04/21/2015 510(K) Number: K040372 |
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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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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 / Light Speed VCT standard configuration, Model 5124069, CT Scanner System. | 2 | 05/15/2007 | GE Healthcare |
GE LightSpeed VCT Select / LightSpeed Pro32, Model 5126093, 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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