510(k) K232242 ยท NFO Stimulator, Transcutaneous Electrical, Aesthetic Purposes
BEAR 2 Body
| Applicant | Foreo, Inc., Las Vegas NV, US |
| Decision | Substantially Equivalent, May 13, 2024 |
| Received | Jul 28, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K232242
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.