ClearanceBrief
510(k) K884394 ยท DTB Permanent Pacemaker Electrode

PACING LEADS FOCUS T81,T81F,T82F,T83,T83F,T84F

ApplicantEla Medical, Inc., Minnetonka MN, US
DecisionSubstantially Equivalent, Dec 8, 1988
ReceivedOct 14, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K884394

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.