510(k) K240564 · NFO Stimulator, Transcutaneous Electrical, Aesthetic Purposes
NuFACE® FIX+
| Applicant | Carol Cole Company Dba Nuface®, Vista CA, US |
| Decision | Substantially Equivalent, Jun 27, 2024 |
| Received | Feb 29, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K240564
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.