ClearanceBrief
510(k) K930542 ยท ESD Hearing Aid, Air-Conduction, Prescription

HEARING AID (ALL-IN-THE-EAR)

ApplicantAction Labs, Inc., Independence MO, US
DecisionSubstantially Equivalent, Apr 7, 1993
ReceivedFeb 2, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K930542

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.