510(k) K062951 ยท LRK Device, Anti-Snoring
TAP III ANTI-SNORING DEVICE
| Applicant | Airway Management, Inc., Dallas TX, US |
| Decision | Substantially Equivalent, Dec 12, 2006 |
| Received | Sep 29, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K062951
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.