Medical Device Recalls
-
11 to 11 of 11 Results
510(K) Number: K092145 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
ARTISTE or ONCOR Linear Accelerators in combination with 160MLC (Multi Leaf Collimator). Linear Acce... | 2 | 06/02/2011 | Siemens Medical Solutions USA, Inc |
-