Medical Device Recalls
-
1 to 4 of 4 Results
510(K) Number: K030420 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
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 |
Lightspeed 16 CT | 2 | 09/21/2015 | GE Healthcare |
GE LightSpeed Pro 16 (100kW/80kW) Models 2357739, 2357739-3, 2357739-4, 2357739-6, 2357739-7 and 235... | 2 | 05/15/2007 | GE Healthcare |
-