Medical Device Recalls
-
|
1 result found
510(K) Number: K232759 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Origin Data Management software versions 3.1.0, 3.1.1, 3.1.2, 3.2.0, 3.2.1 | 2 | 03/18/2025 | Brainlab AG |
-







