510(k) K971818 ยท LQZ Device, Jaw Repositioning
SNOREX
| Applicant | Snorex (Nz) , Ltd., Springfield VA, US |
| Decision | Substantially Equivalent, Dec 18, 1997 |
| Received | May 16, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K971818
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.