510(k) K113569 ยท LRK Device, Anti-Snoring
APNEARX
| Applicant | Apnea Science Corporation, Aliso Viejo CA, US |
| Decision | Substantially Equivalent, Mar 1, 2012 |
| Received | Dec 2, 2011 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K113569
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.