ClearanceBrief
510(k) K782082 ยท DQO Catheter, Intravascular, Diagnostic

CATHETER, DIGITAL POSITRAL II

ApplicantC.R. Bard, Inc., Warrendale PA, US
DecisionSubstantially Equivalent, Dec 20, 1978
ReceivedDec 14, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K782082

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.