ClearanceBrief
510(k) K772238 ยท DXY Implantable Pacemaker Pulse-Generator

PULSE GENERATOR, UNIPOLAR, PROGRAMABLE

ApplicantCardiac Pacemakers, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Jan 30, 1978
ReceivedDec 8, 1977
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K772238

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.