510(k) K223624 ยท LRK Device, Anti-Snoring
Emerald Herbst
| Applicant | Island Dental Lab, Inc Dba Emerald Dental, Valley Stream NY, US |
| Decision | Substantially Equivalent, May 10, 2023 |
| Received | Dec 5, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223624
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.