ClearanceBrief
510(k) K880349 ยท ESD Hearing Aid, Air-Conduction, Prescription

MODEL 759 CUSTOM IN-THE-EAR HEARING AID

ApplicantBernafon, Inc., Mountainside NJ, US
DecisionSubstantially Equivalent, Mar 7, 1988
ReceivedJan 26, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K880349

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.