Medical Device Recalls
-
1 result found
510(K) Number: K141283 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Eclipse Treatment Planning System version 13.MR2 [13.06.31 with Smart Segmentation Knowledge Based ... | 2 | 01/10/2017 | Varian Medical Systems, Inc. |
-