510(k) K093203 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
CARDIOBLATE BIPOLAR RADIOFREQUENCY SURGICAL ABLATION SYSTEM, MODELS 60831, 60832, 60841
| Applicant | Medtronic, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Feb 26, 2010 |
| Received | Oct 13, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K093203
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.