ClearanceBrief
510(k) K181586 ยท KLW Masker, Tinnitus

Tinnitus Sound Generator Module

ApplicantGN Hearing A/S, Ballerup, DK
DecisionSubstantially Equivalent, Jul 13, 2018
ReceivedJun 15, 2018
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K181586

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.