ClearanceBrief
510(k) K861368 ยท JOQ Generator, Pulse, Pacemaker, External Programmable (For Electrophysiological Studies Only)

MEDTRONIC MODEL 5328 PROGRAMMABLE STIMULATOR

ApplicantMedtronic Vascular, Minneapolis MN, US
DecisionSubstantially Equivalent, Aug 4, 1986
ReceivedApr 11, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K861368

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.