ClearanceBrief
510(k) K803286 ยท KRE Analyzer, Pacemaker Generator Function, Indirect

CARDIOMEMO

ApplicantInstromedix, Inc., Walker MI, US
DecisionSubstantially Equivalent, Mar 17, 1981
ReceivedDec 30, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K803286

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.