ClearanceBrief
510(k) K926092 ยท ESD Hearing Aid, Air-Conduction, Prescription

MIRACLE-EAR MODEL HL

ApplicantMiracle-Ear, Inc., Golden Valley MN, US
DecisionSubstantially Equivalent, Feb 12, 1993
ReceivedDec 2, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K926092

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.