510(k) K171243 ยท KLW Masker, Tinnitus
audifon Tinnitus-Module
| Applicant | Audiofon USA, Inc., Debary FL, US |
| Decision | Substantially Equivalent, Oct 19, 2017 |
| Received | Apr 28, 2017 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K171243
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.