ClearanceBrief
510(k) K844793 ยท DXY Implantable Pacemaker Pulse-Generator

SUPRIMA 253-21 IMPLANTABLE PULSE GENERATOR

ApplicantIntermedics, Inc., Freeport TX, US
DecisionSubstantially Equivalent, Feb 8, 1985
ReceivedDec 10, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K844793

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.