510(k) K991209 ยท LRK Device, Anti-Snoring
ORAL SLEEP DISORDER AID
| Applicant | Perl-Rad Sleep Disorder Lab, Carmel CA, US |
| Decision | Substantially Equivalent, Sep 22, 1999 |
| Received | Apr 9, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K991209
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.