ClearanceBrief
510(k) K130855 ยท DYB Introducer, Catheter

PTFE SUPER SHEATH INTRODUCER

ApplicantMartech Medical Products, Harleysville PA, US
DecisionSubstantially Equivalent, Jul 29, 2013
ReceivedMar 28, 2013
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K130855

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.