510(k) K222872 ยท LRK Device, Anti-Snoring
DNA Appliance
| Applicant | Vivos Therapeutics, Inc., Murray KY, US |
| Decision | Substantially Equivalent, Dec 30, 2022 |
| Received | Sep 22, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222872
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.