510(k) K162652 ยท NFO Stimulator, Transcutaneous Electrical, Aesthetic Purposes
Smart Photon Micro-current Device, Model: EP-300
| Applicant | Li-Tek Electronic Technology Corporation, Dongguan, CN |
| Decision | Substantially Equivalent, Oct 25, 2017 |
| Received | Sep 23, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162652
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.