ClearanceBrief
510(k) K973442 ยท IKT Electrode, Needle, Diagnostic Electromyograph

TECA DISPOSABLE MONOPOLAR NEEDLE ELECTRODES

ApplicantMedelec, Inc. D.B.A. Teca Corp., Pleasantville NY, US
DecisionSubstantially Equivalent, Nov 20, 1997
ReceivedSep 11, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K973442

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.