510(k) K112766 ยท LQZ Device, Jaw Repositioning
SNORKEL
| Applicant | Fellmar Company, Monrovia CA, US |
| Decision | Substantially Equivalent, Jun 4, 2012 |
| Received | Sep 22, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K112766
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.