510(k) K880956 ยท LQZ Device, Jaw Repositioning
SNOAR(TM) OPEN AIRWAY APPLIANCE
| Applicant | Kent J. Toone, D.D.S., Cupertino CA, US |
| Decision | Substantially Equivalent, May 11, 1988 |
| Received | Mar 7, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880956
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.