Medical Device Recalls
-
1 result found
510(K) Number: K170086 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Pinnacle3 Radiation Therapy Planning System, Model numbers 870231 and 870237. | 2 | 09/15/2022 | Philips Medical Systems (Cleveland) Inc |
-