ClearanceBrief
510(k) K855103 ยท DQO Catheter, Intravascular, Diagnostic

CIRIBART GYUDUBG CATGETER

ApplicantMansfield Scientific, Inc., Mansfield MA, US
DecisionSubstantially Equivalent, Feb 18, 1986
ReceivedDec 23, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K855103

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.