ClearanceBrief
510(k) K030791 ยท KLW Masker, Tinnitus

ANMP (ACOUSTIC NEURO MODULATION PROTOCOL)

ApplicantTinnitech, Ltd., Sydney, AU
DecisionSubstantially Equivalent, Apr 17, 2003
ReceivedMar 12, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K030791

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.