ClearanceBrief
510(k) K103186 ยท MKJ Automated External Defibrillators (Non-Wearable)

SKINTACT RADIOTRANSPARENT MULTIFUNCTION ELECTRODES

ApplicantLeonhard Lang GmbH, Stillwater MN, US
DecisionSubstantially Equivalent, Feb 8, 2011
ReceivedOct 29, 2010
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K103186

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.