ClearanceBrief
510(k) K781326 ยท DTB Permanent Pacemaker Electrode

UNIPOPLAR ENDOCARDIAL LEADS

ApplicantAmerican Technology, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Dec 4, 1978
ReceivedAug 1, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K781326

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.