510(k) K201782 ยท NFO Stimulator, Transcutaneous Electrical, Aesthetic Purposes
NuFace Trinity Plus Device
| Applicant | Carol Cole Company Dba Nuface, Vista CA, US |
| Decision | Substantially Equivalent, Jan 22, 2021 |
| Received | Jun 30, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K201782
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.