ClearanceBrief
510(k) K982432 ยท KLW Masker, Tinnitus

PILLOW MASKER, C2007M, C2008M,CE2000, WONDER EAR, MINI WONDER EAR, PT-2SM, PT-3SM, PT-3LFM, PT-3HFM, PT3CM, PT5-SM, PT5-

ApplicantTinnitus Treatment Centers, Inc., Dallas TX, US
DecisionSubstantially Equivalent, Jan 25, 1999
ReceivedJul 13, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K982432

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.