ClearanceBrief
510(k) K081878 ยท DQY Catheter, Percutaneous

LEMAITRE TT TORTUOUS TRACKER INTRODUCER CATHETER DELIVERY SYSTEM

ApplicantLeMaitre Vascular, Inc., Burlington MA, US
DecisionSubstantially Equivalent, Jan 27, 2009
ReceivedJul 2, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K081878

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.