510(k) K122391 ยท LRK Device, Anti-Snoring
MEDTRONIC XOMED, INC.
| Applicant | Medtronic Xomed, Inc., Jacksonville FL, US |
| Decision | Substantially Equivalent, Jan 10, 2013 |
| Received | Aug 7, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K122391
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.