ClearanceBrief
510(k) K193303 ยท KLW Masker, Tinnitus

Tinnitus Sound Generator Module

ApplicantGN Hearing A/S, Ballerup, DK
DecisionSubstantially Equivalent, Feb 20, 2020
ReceivedNov 29, 2019
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K193303

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.