CYTOBRUSH

CYTOBRUSH is an FDA 510(k)-cleared medical device (K890706) manufactured by Laboratoire Ccd C/O Washington Regulatory Services. 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 April 24, 1989. Regulation: 8.