ClearanceBrief
510(k) K904547 ยท LDE Stethoscope, Manual

STETHOSCOPE

ApplicantKimball Industries Co., Ltd., Shirley NY, US
DecisionSubstantially Equivalent, Mar 21, 1991
ReceivedOct 3, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K904547

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.