ClearanceBrief
510(k) K915480 ยท DWD Suction Control, Intracardiac, Cardiopulmonary Bypass

B-D ULTRA-VUE PROCEDURE NEEDLE W/ SPINAL TYPE PT.

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic, Franklin Lakes NJ, US
DecisionSubstantially Equivalent, Jan 7, 1992
ReceivedDec 6, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K915480

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.