ClearanceBrief
510(k) K891988 ยท EWO Audiometer

AMPLAID A308 CLINICAL AUDIOMETER

ApplicantAmplus Corp., Boulder CO, US
DecisionSubstantially Equivalent, Oct 12, 1989
ReceivedMar 28, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K891988

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.