ClearanceBrief
510(k) K955882 ยท MKJ Automated External Defibrillators (Non-Wearable)

MEDI-TRACE COMBINATION DEFIBRILLATION & ECG ELECTRODE FOR HEWLETT PACKARD DEFIBRILLATORS

ApplicantGraphic Controls Corp., Buafflo NY, US
DecisionSubstantially Equivalent, Oct 24, 1996
ReceivedDec 28, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K955882

DateFirm and productCodeLinked 510(k)
Oct 15, 2014Covidien LLC
Covidien Kendall 1710H Multi-Function Defibrillation Electrodes Part Number: 40000006
Terminated
MKJNone listed
Oct 15, 2014Covidien LLC
MediChoice Multifunction Electrode Part Number: MC171 OH
Terminated
MKJNone listed

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