Medical Device Recalls
-
|
11 to 14 of 14 Results
510(K) Number: K024012 |
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| GE OEC 9800 Fluoro C-Arm X-ray System, GE OEC Medical Systems Inc. | 2 | 09/30/2006 |
FEI # 1720753 GE OEC Medical Systems, Inc |
| GE OEC 9800 Fluoroscopic X-Ray System, GE Healthcare, Surgery, Salt Lake City, Utah. The intended u... | 2 | 09/25/2008 |
FEI # 1720753 OEC Medical Systems, Inc |
| GE OEC 9900 Elite Fluoroscopic X-Ray System, GE Healthcare, Surgery, Salt Lake City, Utah. The inte... | 2 | 09/25/2008 |
FEI # 1720753 OEC Medical Systems, Inc |
| OEC 9800 Image Intensified fluoroscopic x-ray system (includes OEC 9800, OEC FluoroTrak 9800 Plus, O... | 2 | 09/01/2008 |
FEI # 1720753 OEC Medical Systems, Inc |
-







