510(k) K090911 ยท LQZ Device, Jaw Repositioning
IST SNORING APPLIANCE
| Applicant | Dental Crafters, Marshfeld WI, US |
| Decision | Substantially Equivalent, Sep 11, 2009 |
| Received | Apr 1, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K090911
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.