510(k) K121761 ยท LRK Device, Anti-Snoring
SOMNOGUARD SP SOFT
| Applicant | Tomed Dr. Toussaint GmbH, Holderness NH, US |
| Decision | Substantially Equivalent, Sep 28, 2012 |
| Received | Jun 15, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K121761
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.