510(k) K932932 ยท LQZ Device, Jaw Repositioning
SNOREMASTER SNORE REMEDY
| Applicant | The Snoremaster Co., Philadelphia PA, US |
| Decision | Substantially Equivalent, Feb 10, 1995 |
| Received | Jun 16, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K932932
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.