510(k) K050592 ยท LRK Device, Anti-Snoring
SOMNOMED MAS RXA
| Applicant | Somnomed, Ltd., Stillwater MN, US |
| Decision | Substantially Equivalent, Jul 12, 2005 |
| Received | Mar 8, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K050592
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.