ClearanceBrief
510(k) K161985 ยท DRA Catheter, Steerable

Steerable Guide Catheter

ApplicantAbbott Vascular, Santa Clara CA, US
DecisionSubstantially Equivalent, Aug 7, 2016
ReceivedJul 19, 2016
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K161985

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.