510(k) K150941 ยท LRK Device, Anti-Snoring
Somnowell Mandibular Advancement Appliance (MAA)
| Applicant | Somnowell , Ltd., London, GB |
| Decision | Substantially Equivalent, May 22, 2015 |
| Received | Apr 8, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150941
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.