510(k) K252531 ยท LRK Device, Anti-Snoring
Myosa (S1H, S1, S2, S3, S1M, S2M); Myosa for Snorers (S1, S1M, S2)
| Applicant | Myofunctional Research Co., Helnsvale, AU |
| Decision | Substantially Equivalent, Mar 2, 2026 |
| Received | Aug 12, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K252531
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.