510(k) K122217 ยท NEY System, Ablation, Microwave And Accessories
CERTUS 140 2.45GHZ ABLATION SYSTEM
| Applicant | Neuwave Medical, Inc., Madision WI, US |
| Decision | Substantially Equivalent, Dec 19, 2012 |
| Received | Jul 25, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K122217
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.