510(k) K191672 ยท NFO Stimulator, Transcutaneous Electrical, Aesthetic Purposes
NuFACE Mini Device
| Applicant | Carol Cole Company Dba Nuface, Vista CA, US |
| Decision | Substantially Equivalent, Oct 15, 2019 |
| Received | Jun 24, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K191672
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.