510(k) K150171 ยท KLW Masker, Tinnitus
Tinnitus Sound Generator Module
| Applicant | Gn Resound A/S, Ballerup, DK |
| Decision | Substantially Equivalent, May 14, 2015 |
| Received | Jan 26, 2015 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K150171
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.