ClearanceBrief
510(k) K110154 ยท MKJ Automated External Defibrillators (Non-Wearable)

ZOLL AED PLUS WITH 2010 AHA GUIDLINES SOFTWARE UPDATE

ApplicantZoll Medical Corporation, World Wide Headquarters, Chelsmford MA, US
DecisionSubstantially Equivalent, Feb 17, 2011
ReceivedJan 19, 2011
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K110154

No recall in the FDA data names this 510(k).

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