Medical Device Recalls
-
1 result found
510(K) Number: K170750 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
RT Elements Software revisions of the RT Elements applications have a specific software version nu... | 2 | 04/21/2019 | Brainlab AG |
-