ClearanceBrief
510(k) K874394 ยท DXY Implantable Pacemaker Pulse-Generator

QUANTUM(R) MODELS 253-19V & 254-20V PULSE GENERA.

ApplicantIntermedics, Inc., Freeport TX, US
DecisionSubstantially Equivalent, Nov 23, 1987
ReceivedOct 28, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K874394

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.