VARIAN ORIGAMI, VERSION 1.0

VARIAN ORIGAMI, VERSION 1.0 is an FDA 510(k)-cleared medical device (K932501) manufactured by Varian Assoc., 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 September 22, 1994. Regulation: 8.