510(k) K080509 ยท OCL Surgical Device, For Cutting, Coagulation, And/Or Ablation Of Tissue, Including Cardiac Tissue
CARDIOBLATE 68000 GNERATOR, BP2 SURGICAL ABLATION DEVICE, LP SURGICAL ABLATION DEVICE, GEMINI-SSURGICAL ABLATION DEVICE
| Applicant | Medtronic, Inc., Brooklyn Park MN, US |
| Decision | Substantially Equivalent, May 5, 2008 |
| Received | Feb 25, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K080509
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.