510(k) K082849 ยท LRK Device, Anti-Snoring
SILENT SLEEP
| Applicant | Craniofacial Pain Center of Idaho, Boise ID, US |
| Decision | Substantially Equivalent, Jul 16, 2009 |
| Received | Sep 29, 2008 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K082849
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.