ClearanceBrief
510(k) K140845 ยท KLW Masker, Tinnitus

LEVO TINNITUS MASKING SOFTWARE DEVICE

ApplicantOtoharmonics Corp, Philedelphia PA, US
DecisionSubstantially Equivalent, Jul 18, 2014
ReceivedApr 2, 2014
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K140845

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.