Medical Device Recalls
-
1 to 7 of 7 Results
510(K) Number: K992506 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
OEC MiniView 6800. MDL Number: D002533 The OEC MiniView 6800 Digital Mobile C-Arm is designed to pr... | 2 | 01/09/2017 | GE OEC Medical Systems, Inc |
OEC® MiniView 6800. The Mini 6800 Digital Mobile C-Arm is designed to provide the physician with ... | 2 | 11/07/2014 | GE OEC Medical Systems, Inc |
OEC MiniView 6800 Mobile; MDL number A349855. Product Usage: The mini 6800 digital mobile c arm ... | 2 | 08/01/2012 | GE OEC Medical Systems, Inc |
OEC 6800 Miniview, Image-intensified fluoroscopic x-ray system used during diagnostic, surgical and ... | 1 | 07/24/2012 | GE OEC Medical Systems, Inc |
OEC Miniview 6800 mobile fluoroscopic x-ray system, GE Healthcare, Surgery, Salt Lake City, Utah. | 2 | 07/03/2007 | OEC Medical Systems, Inc |
GE OEC 6800 Fluoroscopic X-ray System, GE Healthcare, Salt Lake City, Utah. | 2 | 06/30/2007 | GE OEC Medical Systems, Inc |
MiniView 6800 Digital Mobile C-arm fluoroscopic x-ray system. | 2 | 09/30/2006 | GE OEC Medical Systems,Inc |
-