510(k) K143591 ยท LRK Device, Anti-Snoring
Dorsal Appliance
| Applicant | Gergens Orthodontic Lab, Phoenix AZ, US |
| Decision | Substantially Equivalent, Apr 15, 2015 |
| Received | Dec 18, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K143591
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.