Medical Device Recalls
-
|
1 result found
510(K) Number: K152928 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Multitom RAX with software version VF10 | 2 | 06/02/2021 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
-







