Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K013561 |
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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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LightSpeed Ultra (8-slice MDAS), 5120327-3 LightSpeed 4.0 CT Scanner System - The LightSpeed 4.0 ... | 2 | 03/04/2016 | GE Medical Systems, LLC |
Lightspeed 16 CT | 2 | 09/21/2015 | GE Healthcare |
CT LightSpeed 16 and Discovery ST Pet/CT DST. Catalogue # 2339985. Designed to be a head and whol... | 2 | 05/15/2015 | GE Healthcare |
GE, VCT for Discovery VCT, Discovery RX VCT, and Discovery PET/CT 690, Lightspeed VCT, Discovery CT7... | 2 | 04/29/2013 | GE Healthcare, LLC |
Performix X-ray Tube - Performix ADV, Performix Ultra, Solarix 630. | 2 | 01/08/2004 | General Electric Med Systems |
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