Medical Device Recalls
-
|
1 to 3 of 3 Results
510(K) Number: K013561 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| LightSpeed Ultra (8-slice MDAS), 5120327-3 LightSpeed 4.0 CT Scanner System - The LightSpeed 4.0 ... | 2 | 03/04/2016 |
FEI # 2126677 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 |
FEI # 2126677 GE Healthcare, LLC |
| CT LightSpeed 16 and Discovery ST Pet/CT DST. Catalogue # 2339985. Designed to be a head and whol... | 2 | 05/15/2015 |
FEI # 2126677 GE Healthcare |
-







