510(k) K160123 ยท LRK Device, Anti-Snoring
Apinator
| Applicant | Allen J. Moses, Dds, Ltd., Chicago IL, US |
| Decision | Substantially Equivalent, Jul 12, 2016 |
| Received | Jan 20, 2016 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K160123
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.