510(k) K191618 ยท LRK Device, Anti-Snoring
SleepTight Mouthpiece STZ
| Applicant | Michael D Williams Dds PA, Davie FL, US |
| Decision | Substantially Equivalent, Dec 11, 2019 |
| Received | Jun 18, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K191618
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.