ClearanceBrief
510(k) K781624 ยท DTB Permanent Pacemaker Electrode

PACING LEAD MODEL BUS 860, BUS 890

ApplicantR.E. Brown Co., Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Dec 21, 1978
ReceivedSep 20, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K781624

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.