ClearanceBrief
510(k) K915495 ยท KMK Device, Intravascular Catheter Securement

DESERET POSITIONAL SUTURE WING

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic, Sandy UT, US
DecisionSubstantially Equivalent, Apr 6, 1992
ReceivedDec 9, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K915495

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.