510(k) K954128 ยท LRK Device, Anti-Snoring
SNOREMASTER
| Applicant | D.D.S., Inc., Half Moon Bay CA, US |
| Decision | Substantially Equivalent, Oct 2, 1995 |
| Received | Sep 1, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K954128
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.