510(k) K211069 ยท LRK Device, Anti-Snoring
EndSnorZ Sleep Appliance
| Applicant | Prismatik Dentalcraft, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Oct 26, 2021 |
| Received | Apr 12, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K211069
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.