ClearanceBrief
510(k) K961013 ยท IKT Electrode, Needle, Diagnostic Electromyograph

DISPOSABLE NEEDLE ELECTRODE

ApplicantMedelec Intl. Corp., England, GB
DecisionSubstantially Equivalent, Dec 20, 1996
ReceivedMar 13, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K961013

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.