ClearanceBrief
510(k) K181042 · DXK Echocardiograph

Ultra ICE Plus – PI 9 MHz Peripheral Imaging Catheter

ApplicantBoston Scientific Corporation, Maple Grove MN, US
DecisionSubstantially Equivalent, May 17, 2018
ReceivedApr 19, 2018
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K181042

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.