510(k) K160141 ยท NEY System, Ablation, Microwave And Accessories
miraDry System
| Applicant | Miramar Labs, Inc., Santa Clara CA, US |
| Decision | Substantially Equivalent, Oct 31, 2016 |
| Received | Jan 21, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160141
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.