ClearanceBrief
510(k) K002280 ยท MKJ Automated External Defibrillators (Non-Wearable)

PAD PRO PEDIATRIC ELECTRODE, MODEL PAD PRO 2602

ApplicantMedical Devices, Inc., Des Moines IA, US
DecisionSubstantially Equivalent, Feb 5, 2001
ReceivedJul 26, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K002280

DateFirm and productCodeLinked 510(k)
Feb 23, 2018ConMed Corporation
MINI INFANT < 3KG, RADIOTRANSLUCENT ELECTRODE, Universal/Anderson Connector, REF/Catalog Number 2602 Indicated for use in external pacing, defibrillation and monitoring applications as a non-sterile,
Terminated		 MKJNone listed
Feb 23, 2018ConMed Corporation
MINI INFANT < 3KG, RADIOTRANSLUCENT ELECTRODE, Philips Plug Style Connector, REF/Catalog Number 2602H Indicated for use in external pacing, defibrillation and monitoring applications as a non-steril
Terminated		 MKJNone listed
Feb 23, 2018ConMed Corporation
MINI INFANT < 3KG, RADIOTRANSLUCENT ELECTRODE, Philips Plug Style Connector, REF/Catalog Number 2602H Indicated for use in external pacing, defibrillation and monitoring applications as a non-steril
Terminated		 MKJNone listed
Feb 23, 2018ConMed Corporation
MINI INFANT < 3KG, RADIOTRANSLUCENT ELECTRODE, Physio-Control Quik-Combo" Connector, REF/Catalog Number 2602M Indicated for use in external pacing, defibrillation and monitoring applications as a no
Terminated		 MKJNone listed
Feb 23, 2018ConMed Corporation
MINI INFANT < 3KG, RADIOTRANSLUCENT ELECTRODE, ZOLL Connector, REF/Catalog Number 2602Z Indicated for use in external pacing, defibrillation and monitoring applications as a non-sterile, disposable
Terminated		 MKJNone listed
Dec 4, 2014ConMed Corporation
MINI PEDIATRIC Radiotransparent Electrode, REF/Catalog Number 2602H, Rx ONLY --- COMPARABLE TO PHILIPS MEDICAL HEARTSTART ELECTRODES PLUG STYLE CONNECTOR--Intended for use during defibrillation, cardi
Terminated		 MKJNone listed

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