Medical Device Recalls
-
|
1 result found
510(K) Number: K994413 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| BrainLab Radiotherapy Treatment Planning Software; Catalog number 20610 - Radiosurgery 3.0 Cata... | 2 | 09/20/2009 | Brainlab AG |
-







