ClearanceBrief
510(k) K895310 ยท EWO Audiometer

AUDIOMETER/MASTER HEARING AID, MAICO MODEL MF7

ApplicantMaico Hearing Instruments, Inc., Minneapolis MN, US
DecisionSubstantially Equivalent, Jan 23, 1990
ReceivedAug 29, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K895310

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.