510(k) K162192 ยท LRK Device, Anti-Snoring
BluePro
| Applicant | Bluesom, Orvault, FR |
| Decision | Substantially Equivalent, Dec 15, 2016 |
| Received | Aug 4, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162192
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.