510(k) K230947 ยท LRK Device, Anti-Snoring
C.A.R.E. Appliance (DNA, mRNA, mmRNA)
| Applicant | Vivos Therapeutics, Inc., Murray KY, US |
| Decision | Substantially Equivalent, Nov 28, 2023 |
| Received | Apr 4, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230947
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.