ClearanceBrief
510(k) K010169 ยท DQY Catheter, Percutaneous

BARD UTRAVERSE SMALL VESSEL PTA BALLOON DILATATION CATHETER

ApplicantC.R. Bard, Inc., Covington GA, US
DecisionSubstantially Equivalent, Feb 13, 2001
ReceivedJan 18, 2001
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K010169

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.