510(k) K223694 ยท KLW Masker, Tinnitus
Tinearity G1 (6103); Tinearity G1 Adapters x3 (6042)
| Applicant | Duearity AB, Malmo, SE |
| Decision | Substantially Equivalent, Jun 30, 2023 |
| Received | Dec 9, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223694
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.