510(k) K111207 ยท LRK Device, Anti-Snoring
RESPIRE BLUE SERIES
| Applicant | Respire Medical, Woodland Hills CA, US |
| Decision | Substantially Equivalent, Aug 23, 2011 |
| Received | Apr 29, 2011 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K111207
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.