510(k) K022284 ยท LRK Device, Anti-Snoring
SNORE-AID MAX
| Applicant | Dental Imagineers, LLC, Ocean NJ, US |
| Decision | Substantially Equivalent, Dec 10, 2002 |
| Received | Jul 15, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K022284
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.