ClearanceBrief
510(k) K822389 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)

LIFE TRACE 40/42

ApplicantLife Science Instrumentation, Inc., Walker MI, US
DecisionSubstantially Equivalent, Sep 21, 1982
ReceivedAug 9, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K822389

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.