510(k) K150566 ยท LRK Device, Anti-Snoring
Oniris
| Applicant | Sas Oniris, Chaville, FR |
| Decision | Substantially Equivalent, Mar 21, 2016 |
| Received | Mar 6, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150566
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.