ClearanceBrief
510(k) K890412 ยท DTB Permanent Pacemaker Electrode

MODELS 430-07 & 431-07 IMPLANTABLE PACING LEADS

ApplicantIntermedics, Inc., Freeport TX, US
DecisionSubstantially Equivalent, Mar 28, 1989
ReceivedJan 24, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K890412

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.