ClearanceBrief
510(k) K782071 ยท DYG Catheter, Flow Directed

CATHETER, USCI GRUNTZIG/BALLOON

ApplicantC.R. Bard, Inc., Warrendale PA, US
DecisionSubstantially Equivalent, Dec 15, 1978
ReceivedDec 13, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K782071

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.