510(k) K130797 ยท LRK Device, Anti-Snoring
LUCO HYBRID OSA APPLIANCE
| Applicant | Luco Hybrid Osa Appliance, Inc., Kingston, CA |
| Decision | Substantially Equivalent, Dec 18, 2013 |
| Received | Mar 22, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K130797
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.