510(k) K060122 ยท LRK Device, Anti-Snoring
SLEEP SPLINT
| Applicant | Nakagawa Dental Clinic, Mineola NY, US |
| Decision | Substantially Equivalent, May 19, 2006 |
| Received | Jan 17, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K060122
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.