Medical Device Recalls
-
|
1 result found
510(K) Number: K200514 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Cardioblate" Gemini"-s Irrigated RF Surgical Ablation System; The device is placed in a plastic tray... | 2 | 05/25/2022 | Medtronic Perfusion Systems |
-







