CYTEX ONE AND CYTEX TWO

CYTEX ONE AND CYTEX TWO is an FDA 510(k)-cleared medical device (K890283) manufactured by Anderson Winn Paper Co.. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 15, 1989. Regulation: 8.