ClearanceBrief
510(k) K163094 ยท KLW Masker, Tinnitus

TinniLogic Mobile Tinnitus Management Device

ApplicantJiangsu Betterlife Medical Co., Ltd., Changshu, CN
DecisionSubstantially Equivalent, May 17, 2017
ReceivedNov 4, 2016
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K163094

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.