510(k) K020893 ยท LRK Device, Anti-Snoring
NORAD NOCTURNAL ORAL AIRWAY DILATOR APPLIANCE
| Applicant | Dennis R. Bailey, Dds, Englewood CO, US |
| Decision | Substantially Equivalent, May 28, 2002 |
| Received | Mar 19, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K020893
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.