ClearanceBrief
510(k) K852432 ยท DXY Implantable Pacemaker Pulse-Generator

SUPRIMA II MODEL 254-28

ApplicantIntermedics, Inc., Freeport TX, US
DecisionSubstantially Equivalent, Jul 17, 1985
ReceivedJun 10, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K852432

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.