ClearanceBrief
510(k) K770938 ยท KLW Masker, Tinnitus

TINNITUS AID, MODEL S244

ApplicantVicon Instrument Co. MD, US
DecisionSubstantially Equivalent, Jun 28, 1977
ReceivedMay 23, 1977
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K770938

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.