510(k) K121285 ยท LRK Device, Anti-Snoring
ORAVAN OSA
| Applicant | New Jersey Snoring Solutions, West Orange NJ, US |
| Decision | Substantially Equivalent, Mar 8, 2013 |
| Received | Apr 30, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K121285
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.