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

B-D ULTRA-VUE PROCEDURE NEEDLE W/ SPINAL TYPE PT. is an FDA 510(k)-cleared medical device (K915480) manufactured by Bd Becton Dickinson Vacutainer Systems Preanalytic. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 6, 1992. Regulation: 8.