510(k) K261366 ยท LRK Device, Anti-Snoring
Virtus
| Applicant | Somnomed, Inc., Plano TX, US |
| Decision | Substantially Equivalent, Jun 12, 2026 |
| Received | Apr 27, 2026 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K261366
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.