ClearanceBrief
510(k) K011826 ยท JOQ Generator, Pulse, Pacemaker, External Programmable (For Electrophysiological Studies Only)

EPS320 CARDIAC STIMULATOR

ApplicantMicropace Pty, Ltd., Campsie, N.S.W., AU
DecisionSubstantially Equivalent, Jan 24, 2002
ReceivedJun 11, 2001
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K011826

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.