TETRAD MODEL BG22, AUTOMATIC BIOPSY UNIT MODEL

TETRAD MODEL BG22, AUTOMATIC BIOPSY UNIT MODEL is an FDA 510(k)-cleared medical device (K945320) manufactured by Tetra Corp.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 10, 1995. Regulation: 8.