510(k) K133823 ยท NFO Stimulator, Transcutaneous Electrical, Aesthetic Purposes
NUFACE MINI DEVICE
| Applicant | Carol Cole Company, Vista CA, US |
| Decision | Substantially Equivalent, Apr 17, 2014 |
| Received | Dec 17, 2013 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K133823
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.