510(k) K182661 ยท LRK Device, Anti-Snoring
Kava and Kava with Herbst
| Applicant | Sketchpad Innovations, LLC, San Diego CA, US |
| Decision | Substantially Equivalent, Feb 13, 2019 |
| Received | Sep 25, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182661
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.