510(k) K162306 ยท LRK Device, Anti-Snoring
SomnoDent ALPHA
| Applicant | Somnomed, Inc., Frisco TX, US |
| Decision | Substantially Equivalent, Sep 20, 2016 |
| Received | Aug 17, 2016 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K162306
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.