ClearanceBrief
510(k) K070743 ยท JOQ Generator, Pulse, Pacemaker, External Programmable (For Electrophysiological Studies Only)

Z6 STIMULATOR

ApplicantSt Cardio Technologies, LLC, Broomfield CO, US
DecisionSubstantially Equivalent, Jul 2, 2007
ReceivedMar 16, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K070743

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.