510(k) K101155 ยท LRK Device, Anti-Snoring
AURADORM (NEUROMUSCULAR SLEEP)
| Applicant | Sleepwright, Santa Fe NM, US |
| Decision | Substantially Equivalent, May 12, 2011 |
| Received | Apr 26, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101155
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.