ClearanceBrief
510(k) K910609 ยท DTB Permanent Pacemaker Electrode

PERMANENT IMPLANTABLE JP ENDOCARDIAL LEADS W/TIP

ApplicantBiotronik, GmbH & Co., Lake Oswego OR, US
DecisionSubstantially Equivalent, Aug 28, 1991
ReceivedFeb 12, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K910609

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.