ClearanceBrief
510(k) K813143 ยท DYB Introducer, Catheter

DESILET

ApplicantExco, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Nov 27, 1981
ReceivedNov 5, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K813143

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.