510(k) K142651 ยท LRK Device, Anti-Snoring
The Moses Express appliance
| Applicant | Allen J. Moses, Dds, Ltd., Chicago IL, US |
| Decision | Substantially Equivalent, Jul 17, 2015 |
| Received | Sep 18, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142651
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.