ClearanceBrief
510(k) K821073 ยท DXY Implantable Pacemaker Pulse-Generator

PULSE GENERATOR

ApplicantBiotronik Sales, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, May 7, 1982
ReceivedApr 16, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K821073

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.