510(k) K221322 ยท LRK Device, Anti-Snoring
CUSTMBITE Snoring System
| Applicant | Dental Choice Holdings, LLC, Louisville KY, US |
| Decision | Substantially Equivalent, Oct 27, 2022 |
| Received | May 6, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K221322
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.