ClearanceBrief
510(k) K060190 ยท DYB Introducer, Catheter

SUPER SHEATH XL INTRODUCER SHEATH

ApplicantTogo Medikit Co., Ltd., Plymouth MN, US
DecisionSubstantially Equivalent, Apr 4, 2006
ReceivedJan 24, 2006
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K060190

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.