510(k) K132506 ยท LRK Device, Anti-Snoring
SLEEPTIGHT MOUTHPIECE, SLEEPPRO, QUIETNITE, ALTITUDE MOUTHPIECE, SLEEP EASY
| Applicant | Michael D Williams Dds PA, Davie FL, US |
| Decision | Substantially Equivalent, May 29, 2014 |
| Received | Aug 12, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K132506
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.