ClearanceBrief
510(k) K112761 ยท MKJ Automated External Defibrillators (Non-Wearable)

ZOLL PROPAQ MD

ApplicantZoll Medical Corporation, World Wide Headquarters, Chelsmford MA, US
DecisionSubstantially Equivalent, Apr 25, 2012
ReceivedSep 22, 2011
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K112761

DateFirm and productCodeLinked 510(k)
Mar 31, 2014ZOLL Medical Corporation
Zoll Medical X Series, PropaqMD, PropaqM Defibrillator/Pacemaker/Monitor With System Software Version 02.10.02.00 or Higher, automated external defibrillator.
Terminated
MKJNone listed

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