ClearanceBrief
510(k) K885267 ยท DXY Implantable Pacemaker Pulse-Generator

VS-1 MODEL NUMBER 251K PULSE GENERATOR

ApplicantPacesetter Systems, Sylmar CA, US
DecisionSubstantially Equivalent, Mar 28, 1989
ReceivedDec 22, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K885267

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.