ClearanceBrief
510(k) K820232 ยท LDF Electrode, Pacemaker, Temporary

TRANSTHORACIC TEMP. PACEMAKER #100TPE

ApplicantTrans Pace, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Apr 9, 1982
ReceivedJan 28, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K820232

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.