510(k) K183443 ยท LRK Device, Anti-Snoring
SomnoDent Avant
| Applicant | Somnomed, Inc., Plano TX, US |
| Decision | Substantially Equivalent, May 8, 2019 |
| Received | Dec 12, 2018 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K183443
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.