510(k) K061865 ยท NEY System, Ablation, Microwave And Accessories
FLEX 10 MIS ABLATION PROBE, MODEL FLX10MI-05
| Applicant | Guidant Corp., Santa Clara CA, US |
| Decision | Substantially Equivalent, Jul 27, 2006 |
| Received | Jul 3, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K061865
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.