510(k) K131138 ยท LRK Device, Anti-Snoring
RESPIRE PINK SERIES - HERBST
| Applicant | Respire Medical, Woodland Hills CA, US |
| Decision | Substantially Equivalent, Sep 9, 2013 |
| Received | Apr 23, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131138
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.