510(k) K130558 ยท LRK Device, Anti-Snoring
SOMNODENT HERBST; CLASSIC, FLEX
| Applicant | Somnomed, Inc., Frisco TX, US |
| Decision | Substantially Equivalent, May 17, 2013 |
| Received | Mar 4, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K130558
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.