510(k) K153200 ยท LRK Device, Anti-Snoring
SnoreRx
| Applicant | Apnea Sciences Corporation, Aliso Viejo CA, US |
| Decision | Substantially Equivalent, Aug 9, 2016 |
| Received | Nov 4, 2015 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K153200
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.