ClearanceBrief
510(k) K900519 ยท DRX Electrode, Electrocardiograph

CLASSIC ECG/STIMULATING NO. 1700 SERIES

ApplicantClassic Medical Products, Inc., Muskego WI, US
DecisionSubstantially Equivalent, Mar 19, 1990
ReceivedFeb 2, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K900519

DateFirm and productCodeLinked 510(k)
Dec 10, 2012Covidien LLC dba Uni-Patch
Reusable, Self-Adhering TENS/NMES/FES electrodes Single Patient Use Only. An electrocardiograph electrode is the electrical conductor which is applied to the surface of the body to transmit the ele
Terminated
GXYNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.