ClearanceBrief
510(k) K031624 ยท KLW Masker, Tinnitus

TINNITUS RX

ApplicantTinnitus Control, Inc., Washington DC, US
DecisionSubstantially Equivalent, Jul 24, 2003
ReceivedMay 23, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K031624

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.