510(k) K963591 ยท LRK Device, Anti-Snoring
SNORING CONTROL DEVICE
| Applicant | Kenneth Hilsen, New York NY, US |
| Decision | Substantially Equivalent, Jan 9, 1998 |
| Received | Sep 9, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K963591
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.