510(k) K021569 ยท LRK Device, Anti-Snoring
RESTFUL NIGHTS, IST-APPLIANCE
| Applicant | Ottawa Dental Laboratory, Crofton MD, US |
| Decision | Substantially Equivalent, Mar 15, 2004 |
| Received | May 14, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K021569
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.