510(k) K190623 ยท OCL Surgical Device, For Cutting, Coagulation, And/Or Ablation Of Tissue, Including Cardiac Tissue
Cardioblate Pen Surgical Ablation Device, Cardioblate XL Pen Surgical Ablation Device
| Applicant | Medtronic, Minneapolis MN, US |
| Decision | Substantially Equivalent, May 30, 2019 |
| Received | Mar 11, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190623
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.