510(k) K070311 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
CARDIOBLATE GEMINI SURGICAL ABLATION DEVICE, MODELS 49260 AND 49261
| Applicant | Medtronic Vascular, Brooklyn Park MN, US |
| Decision | Substantially Equivalent, Apr 24, 2007 |
| Received | Feb 1, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070311
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.