510(k) K163580 ยท LRK Device, Anti-Snoring
ASD Oral Appliances
| Applicant | American Sleep Dentistry, Cedar City UT, US |
| Decision | Substantially Equivalent, Jun 8, 2017 |
| Received | Dec 20, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K163580
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.