510(k) K231138 ยท LRK Device, Anti-Snoring
Aniti-Snore Mouthguard+
| Applicant | Oscimed SA, Suisse, CH |
| Decision | Substantially Equivalent, Jan 16, 2024 |
| Received | Apr 21, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K231138
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.