ClearanceBrief
510(k) K960031 ยท ESD Hearing Aid, Air-Conduction, Prescription

AUDIOFLEX 120

ApplicantMaico Hearing Instruments, Inc., Minneapolis MN, US
DecisionSubstantially Equivalent, Mar 7, 1996
ReceivedJan 2, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K960031

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.