510(k) K132933 ยท LRK Device, Anti-Snoring
THE MOSES ELITE APPLIANCE
| Applicant | Allen J. Moses, Dds, Ltd., Chicago IL, US |
| Decision | Substantially Equivalent, Apr 25, 2014 |
| Received | Sep 18, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K132933
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.