510(k) K870501 ยท LQZ Device, Jaw Repositioning
THE EQUALIZER AIRWAY DEVICE
| Applicant | Sleep Renewal, Inc., Mobile AL, US |
| Decision | Substantially Equivalent, Mar 4, 1987 |
| Received | Feb 4, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K870501
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.