510(k) K181123 ยท LRK Device, Anti-Snoring
ApnoDent Appliance
| Applicant | Apnomed, Inc., Bellevue WA, US |
| Decision | Substantially Equivalent, Nov 21, 2018 |
| Received | Apr 30, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181123
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.