ClearanceBrief
510(k) K020288 ยท MKJ Automated External Defibrillators (Non-Wearable)

PADPRO, MODEL 2603

ApplicantPadpro, LLC, Deer Field IL, US
DecisionSubstantially Equivalent, Feb 27, 2002
ReceivedJan 28, 2002
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K020288

DateFirm and productCodeLinked 510(k)
Dec 4, 2014ConMed Corporation
PEDIATRIC Radiotransparent Electrode, REF/Catalog Number 2603H, Rx ONLY --- COMPARABLE TO PHILIPS MEDICAL HEARTSTART ELECTRODES PLUG STYLE CONNECTOR
Terminated
MKJNone listed

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