ClearanceBrief
510(k) K970719 ยท MKJ Automated External Defibrillators (Non-Wearable)

700-MP DISPOSABLE RADIOLUCENT MULTI-PAD ELECTRODES

ApplicantCardiotronics Systems, Inc., Carlsbad CA, US
DecisionSubstantially Equivalent, Apr 16, 1997
ReceivedFeb 27, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K970719

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.