510(k) K121878 ยท OCL Surgical Device, For Cutting, Coagulation, And/Or Ablation Of Tissue, Including Cardiac Tissue
CARDIOBLATE CRYOFLEX SURGICAL ABLATION PROBES
| Applicant | Medtronic, Inc., Mounds View MN, US |
| Decision | Substantially Equivalent, Nov 2, 2012 |
| Received | Jun 28, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K121878
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.