510(k) K013808 ยท LRK Device, Anti-Snoring
SLEEPBITE
| Applicant | Dental Imagineers, LLC, Ocean NJ, US |
| Decision | Substantially Equivalent, Jan 30, 2002 |
| Received | Nov 15, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013808
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.