510(k) K170692 ยท LRK Device, Anti-Snoring
Respire Pink Series with DentiTrac
| Applicant | Respire Medical Holding, Brooklyn NY, US |
| Decision | Substantially Equivalent, May 26, 2017 |
| Received | Mar 7, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170692
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.