510(k) K151558 ยท KLW Masker, Tinnitus
Desyncra for Tinnitus Therapy System, Desyncra for Tinnitus Pro System
| Applicant | Neurotherapies Reset GmbH, Juelich, DE |
| Decision | Substantially Equivalent, Jan 20, 2016 |
| Received | Jun 10, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K151558
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.