ClearanceBrief
510(k) K984286 ยท MKJ Automated External Defibrillators (Non-Wearable)

HEARTSTREAM ELECTRODE ADAPTER

ApplicantHewlett-Packard Co., Seattle WA, US
DecisionSubstantially Equivalent, Dec 17, 1998
ReceivedDec 1, 1998
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K984286

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.