ClearanceBrief
510(k) K093715 ยท KLW Masker, Tinnitus

EVOK 900 SERIES HEARING AID/TINNITUS MASKER OPTION DEVICE

ApplicantMagnatone Hearing Aid Corp. Dba Persona Medical, Casselberry FL, US
DecisionSubstantially Equivalent, Dec 22, 2010
ReceivedDec 1, 2009
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K093715

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.