510(k) K182610 ยท OCL Surgical Device, For Cutting, Coagulation, And/Or Ablation Of Tissue, Including Cardiac Tissue
Valleylab FT10 Electrosurgical Platform, Cardioblate BP2 Surgical Ablation Device, Cardioblate LP Surgical Ablation Device
| Applicant | Medtronic, Minneapolis MN, US |
| Decision | Substantially Equivalent, Dec 19, 2018 |
| Received | Sep 21, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182610
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.