510(k) K102521 ยท LRK Device, Anti-Snoring
PANTINO PRO POSITINER
| Applicant | Somnomed, Inc., Denton TX, US |
| Decision | Substantially Equivalent, Mar 28, 2011 |
| Received | Sep 2, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K102521
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.