510(k) K882303 ยท LRK Device, Anti-Snoring
H&M ANTI-SNORING DEVICE
| Applicant | Hays & Meade, Inc., Albuquerque NM, US |
| Decision | Substantially Equivalent, Apr 14, 1989 |
| Received | Jun 3, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882303
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.