510(k) K152159 ยท LRK Device, Anti-Snoring
Oravan Herbst
| Applicant | Oravanosa, LLC, West Orange NJ, US |
| Decision | Substantially Equivalent, Oct 29, 2015 |
| Received | Aug 3, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K152159
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.