510(k) K151719 ยท KLW Masker, Tinnitus
REVE134
| Applicant | Kw Ear Lab, Inc., Carson CA, US |
| Decision | Substantially Equivalent, Oct 9, 2015 |
| Received | Jun 25, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K151719
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.