510(k) K162816 ยท LQZ Device, Jaw Repositioning
SML-OSA2 Appliances
| Applicant | Selane Products, Inc., Chatsworth CA, US |
| Decision | Substantially Equivalent, Jul 27, 2017 |
| Received | Oct 6, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162816
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.