510(k) K061688 ยท LRK Device, Anti-Snoring
ANTI-SNORING / SLEEP APNEA DEVICE
| Applicant | Tomed Dr. Toussaint GmbH, Bensheim, DE |
| Decision | Substantially Equivalent, Sep 8, 2006 |
| Received | Jun 15, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K061688
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.