510(k) K022891 ยท LRK Device, Anti-Snoring
THE BREATHE EZ ANTI-SNORING DEVICE
| Applicant | D&S Redhage, New Haven MO, US |
| Decision | Substantially Equivalent, Feb 19, 2003 |
| Received | Aug 30, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K022891
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.