ClearanceBrief
510(k) K131332 ยท DYB Introducer, Catheter

CARDIOSOLUTIONS PERCU-PRO STEERABLE INTRODUCER

ApplicantCardiosolutions, Inc., West Bridgewater MA, US
DecisionSubstantially Equivalent, Jul 19, 2013
ReceivedMay 9, 2013
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K131332

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.