510(k) K011723 ยท LRK Device, Anti-Snoring
ANTI-SNORING DEVICE OR ASD
| Applicant | Pi Medical, Minneapolis MN, US |
| Decision | Substantially Equivalent, Dec 18, 2002 |
| Received | Jun 4, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K011723
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.