ClearanceBrief
510(k) K901783 ยท ESD Hearing Aid, Air-Conduction, Prescription

AUDIOTONE ITE HEARING AID MODEL ZA (MICRO)

ApplicantMiracle-Ear, Inc., Minneapolis MN, US
DecisionSubstantially Equivalent, May 29, 1990
ReceivedApr 17, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K901783

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.