ClearanceBrief
510(k) K851091 ยท JOQ Generator, Pulse, Pacemaker, External Programmable (For Electrophysiological Studies Only)

MEDTRONIC MODEL 5328 PROGRAM-STIMULATOR

ApplicantMedtronic Vascular, Minneapolis MN, US
DecisionSubstantially Equivalent, Apr 16, 1985
ReceivedMar 18, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K851091

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.