AUTOMATIC TRAY (ACT I & ACT II

AUTOMATIC TRAY (ACT I & ACT II is an FDA 510(k)-cleared medical device (K820117) manufactured by Burbury & Cutter Ind., Inc.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 17, 1982. Regulation: 8.