510(k) K041340 ยท NEY System, Ablation, Microwave And Accessories
GUIDANT MICROWAVE ABLATION SYSTEM
| Applicant | Guidant Corporation, Cardiac Surgery, Santa Clara CA, US |
| Decision | Substantially Equivalent, Jul 28, 2004 |
| Received | May 20, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K041340
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.