510(k) K111110 ยท LRK Device, Anti-Snoring
APNEA GUARD
| Applicant | Advanced Brain Monitoring, Inc., Bonita Springs FL, US |
| Decision | Substantially Equivalent, Jul 22, 2011 |
| Received | Apr 20, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K111110
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.