ClearanceBrief
510(k) K132545 ยท DQX Wire, Guide, Catheter

MEDIVALVE ACWIRE

ApplicantMedivalve , Ltd., Providence RI, US
DecisionSubstantially Equivalent, Nov 8, 2013
ReceivedAug 13, 2013
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K132545

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.