ClearanceBrief
510(k) K942722 ยท LRB Face Plate Hearing Aid

MODULE PROGRAM

ApplicantElectone, Inc., Winter Park FL, US
DecisionSubstantially Equivalent, Sep 6, 1994
ReceivedJun 9, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K942722

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.