510(k) K232735 ยท LRK Device, Anti-Snoring
EMA 3D
| Applicant | Ema Sleep Incorporated, Spicewood TX, US |
| Decision | Substantially Equivalent, May 3, 2024 |
| Received | Sep 7, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K232735
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.