510(k) K073004 ยท LRK Device, Anti-Snoring
SOMNOMED BFLEX
| Applicant | Somnomed, Inc., Denton TX, US |
| Decision | Substantially Equivalent, Jan 30, 2008 |
| Received | Oct 24, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K073004
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.