510(k) K121344 ยท LRK Device, Anti-Snoring
NU SLEEP
| Applicant | Rh Associates, LLC, Woodland Hills CA, US |
| Decision | Substantially Equivalent, Oct 17, 2012 |
| Received | May 4, 2012 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K121344
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.