ClearanceBrief
510(k) K925143 ยท DTE Pulse-Generator, Pacemaker, External

MODEL 4800 ACCUPACE PACING SYSTEM ANALYER

ApplicantPace Medical, Waltham MA, US
DecisionSubstantially Equivalent, Sep 27, 1994
ReceivedOct 13, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K925143

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.