BREAST LESION LOCALIZATION NEEDLE

BREAST LESION LOCALIZATION NEEDLE is an FDA 510(k)-cleared medical device (K881697) manufactured by Bd Becton Dickinson Vacutainer Systems Preanalytic. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 13, 1988. Regulation: 8.