ClearanceBrief
510(k) K831854 ยท DYG Catheter, Flow Directed

USCI ANGIOGRAPHIC BALLOON CATHETER

ApplicantC.R. Bard, Inc., Warrendale PA, US
DecisionSubstantially Equivalent, Oct 20, 1983
ReceivedJun 9, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K831854

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.