510(k) K093710 ยท LRK Device, Anti-Snoring
THE MOSES APPLIANCE
| Applicant | Allen J. Moses, Dds, Ltd., Chicago IL, US |
| Decision | Substantially Equivalent, May 12, 2010 |
| Received | Dec 2, 2009 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K093710
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.