ClearanceBrief
510(k) K813510 ยท LDE Stethoscope, Manual

CARDIOSONIC ACOUSTIC AMPLIFIER

ApplicantSrs Co., Mchenry IL, US
DecisionSubstantially Equivalent, Jan 12, 1982
ReceivedDec 15, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K813510

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.