510(k) K033822 ยท LRK Device, Anti-Snoring
RESPIRONICS CUSTOM I ORAL APPLIANCE
| Applicant | Respironics, Inc., Murrysville PA, US |
| Decision | Substantially Equivalent, Feb 6, 2004 |
| Received | Dec 10, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K033822
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.