ClearanceBrief
510(k) K930770 ยท DXY Implantable Pacemaker Pulse-Generator

MEDTRONIC MINIX & MINIX ST PULSE GENERATORS

ApplicantMedtronic Vascular, Minneapolis MN, US
DecisionSubstantially Equivalent, May 14, 1993
ReceivedFeb 16, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K930770

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.