ClearanceBrief
510(k) K850763 ยท ESD Hearing Aid, Air-Conduction, Prescription

EARETTE HEARING AID OTICON E32U

ApplicantOticon Corp., Somerset NJ, US
DecisionSubstantially Equivalent, Mar 25, 1985
ReceivedFeb 25, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K850763

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.