ClearanceBrief
510(k) K800356 ยท DYB Introducer, Catheter

PERMANENT LEAD INTRADUCER

ApplicantDaig Corp., Mchenry IL, US
DecisionSubstantially Equivalent, May 28, 1980
ReceivedFeb 15, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K800356

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.