ClearanceBrief
510(k) K800891 ยท DTB Permanent Pacemaker Electrode

RESTERILIZATION OF IMPLANTABLE ELECTRODE

ApplicantTelectronics, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, May 28, 1980
ReceivedApr 18, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K800891

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.