Medical Device Recalls
-
1 result found
510(K) Number: K181404 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Varian Multileaf Collimator [MLC]; Millenium Multileaf Collimator [52, 80, 120 leaf]; High Definitio... | 2 | 05/05/2020 | Varian Medical Systems, Inc. |
-