510(k) K030440 ยท LRK Device, Anti-Snoring
OASYS-ORAL AIRWAY SYSTEM
| Applicant | Mark Abramson, D.D.S., Inc., Redwood City CA, US |
| Decision | Substantially Equivalent, Aug 26, 2003 |
| Received | Feb 11, 2003 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K030440
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.