ClearanceBrief
510(k) K971080 ยท EWO Audiometer

MAICO MA52

ApplicantBernafon-Maico, Inc., Eden Prairie MN, US
DecisionSubstantially Equivalent, Jun 6, 1997
ReceivedMar 25, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K971080

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.