510(k) K954324 ยท LRK Device, Anti-Snoring
SNOR-X MOUTH GUARD
| Applicant | Snorex, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Oct 17, 1995 |
| Received | Sep 18, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K954324
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.