510(k) K092942 ยท LRK Device, Anti-Snoring
VITAL SLEEP
| Applicant | The Snore Reliever Company, LLC, Laguna Niguel CA, US |
| Decision | Substantially Equivalent, Jan 13, 2010 |
| Received | Sep 24, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K092942
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.