510(k) K152292 ยท LRK Device, Anti-Snoring
Respire Blue Series-EF
| Applicant | Respire Medical Holding, Brooklyn NY, US |
| Decision | Substantially Equivalent, Dec 7, 2015 |
| Received | Aug 13, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K152292
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.