ClearanceBrief
510(k) K884811 ยท DTB Permanent Pacemaker Electrode

ACCUFIX AND LASERDISH BIPOLAR VS-1 LEADS

ApplicantTelectronics and Control Pacing Systems, Englewood CO, US
DecisionSubstantially Equivalent, Feb 22, 1989
ReceivedNov 17, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K884811

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.