510(k) K973884 ยท LRK Device, Anti-Snoring
ELASTIC MANDIBULAR ADVANCEMENT - TITRATION (EMA-T) APPILANCE
| Applicant | Frantz Design, Inc., Webster TX, US |
| Decision | Substantially Equivalent, Jan 9, 1998 |
| Received | Oct 14, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K973884
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.