510(k) K161980 ยท LRK Device, Anti-Snoring
Fuselier Intraoral Nighttime Device (FIND)
| Applicant | Fuselier Enterprises, LLC, Maitland FL, US |
| Decision | Substantially Equivalent, Feb 7, 2017 |
| Received | Jul 18, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K161980
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.