510(k) K192127 ยท LRK Device, Anti-Snoring
Respire Pink AT (Hard, Hard/Soft, EF)
| Applicant | Respire Medical Holdings, Brooklyn NY, US |
| Decision | Substantially Equivalent, Feb 5, 2020 |
| Received | Aug 6, 2019 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K192127
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.