510(k) K133683 ยท LRK Device, Anti-Snoring
MICR02 OSA DEVICE
| Applicant | Microdental, Inc., Dublin CA, US |
| Decision | Substantially Equivalent, Jul 24, 2014 |
| Received | Dec 2, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133683
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.