ClearanceBrief
510(k) K800702 ยท KLW Masker, Tinnitus

TA-641 TINNITUS INSTRUMENT

ApplicantAudiotrone, Walker MI, US
DecisionSubstantially Equivalent, May 8, 1980
ReceivedMar 28, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K800702

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.