510(k) K180691 ยท LRK Device, Anti-Snoring
TrueDorsal Devices
| Applicant | True Function Laboratory, Inc., La Mesa CA, US |
| Decision | Substantially Equivalent, Feb 11, 2019 |
| Received | Mar 16, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180691
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.