ClearanceBrief
510(k) K990015 ยท IKT Electrode, Needle, Diagnostic Electromyograph

ELECTRODE NEEDLES

ApplicantTechnomed Europe, 6191 Bg Beek, NL
DecisionSubstantially Equivalent, May 27, 1999
ReceivedJan 4, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K990015

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.