ClearanceBrief
510(k) K781822 ยท DTD Pacemaker Lead Adaptor

ELECTRODE, MODEL 030-324

ApplicantTelectronics, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Feb 8, 1979
ReceivedOct 27, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K781822

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.