ClearanceBrief
510(k) K781349 ยท DTC Analyzer, Pacemaker Generator Function

PACER-TRACER PULSE WIDTH

ApplicantInstromedix, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Aug 31, 1978
ReceivedAug 7, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K781349

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.