510(k) K062333 ยท LRK Device, Anti-Snoring
LAIMAD
| Applicant | Steven Lamberg, D.D.S, Washington DC, US |
| Decision | Substantially Equivalent, Dec 14, 2006 |
| Received | Aug 10, 2006 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K062333
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.