510(k) K133390 ยท LRK Device, Anti-Snoring
NDX DORSAL APPLIANCE
| Applicant | Institute For Quality Resource Management, St. Louis MO, US |
| Decision | Substantially Equivalent, Oct 16, 2014 |
| Received | Nov 5, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133390
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.