Medical Device Recalls
-
|
1 to 2 of 2 Results
510(K) Number: K233669 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| OEC 3D | 2 | 06/09/2025 | GE Medical Systems, LLC |
| OEC 3D REF Image-Intensified Fluoroscopic X-Ray System, Mobile. The OEC 3D is a mobile fluorosco... | 2 | 12/18/2024 | GE OEC Medical Systems, Inc |
-







