510(k) K012142 ยท LRK Device, Anti-Snoring
THE QUIET SLEEPER
| Applicant | Precision Dental Laboratories, Inc., Fargo ND, US |
| Decision | Substantially Equivalent, Oct 4, 2001 |
| Received | Jul 10, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K012142
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.