510(k) K200803 ยท NFO Stimulator, Transcutaneous Electrical, Aesthetic Purposes
BEAR and BEAR mini
| Applicant | Foreo, Inc., Las Vegas NV, US |
| Decision | Substantially Equivalent, Jul 31, 2020 |
| Received | Mar 27, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K200803
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.