ClearanceBrief
510(k) K900553 ยท JOQ Generator, Pulse, Pacemaker, External Programmable (For Electrophysiological Studies Only)

CONSTANT CURRENT STIMULATOR MODEL 022101

ApplicantEp Technologies, Inc., Mountain View CA, US
DecisionSubstantially Equivalent, Mar 13, 1990
ReceivedFeb 6, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K900553

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.