510(k) K214100 ยท NFO Stimulator, Transcutaneous Electrical, Aesthetic Purposes
Luminice
| Applicant | Premier North America, Inc., Fort Lauderdale FL, US |
| Decision | Substantially Equivalent, Feb 24, 2022 |
| Received | Dec 29, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K214100
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.