510(k) K253868 ยท LRK Device, Anti-Snoring
QuietLab Pro
| Applicant | QuietLab, LLC, New York NY, US |
| Decision | Substantially Equivalent, Dec 5, 2025 |
| Received | Dec 3, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K253868
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.