ClearanceBrief
510(k) K061111 ยท KLW Masker, Tinnitus

TINNITUS PHASE-OUT

ApplicantTinnitus Control, Inc., Washington DC, US
DecisionSubstantially Equivalent, May 16, 2006
ReceivedApr 21, 2006
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K061111

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.