ClearanceBrief
510(k) K992372 ยท IKD Cable, Electrode

THE LEADAWAY

ApplicantTherapy Equipment, Inc., West Palm Beach FL, US
DecisionSubstantially Equivalent, Oct 13, 1999
ReceivedJul 15, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K992372

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.