ClearanceBrief
510(k) K901386 ยท ESD Hearing Aid, Air-Conduction, Prescription

SEARS MODEL LS9093 IN-THE-EAR HEARING INSTRUMENT

ApplicantMiracle-Ear, Inc., Golden Valley MN, US
DecisionSubstantially Equivalent, Apr 13, 1990
ReceivedMar 26, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K901386

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.