VISION TWO, ONE/10 ONE/20 &24

VISION TWO, ONE/10 ONE/20 &24 is an FDA 510(k)-cleared medical device (K832895) manufactured by Comtal 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 December 7, 1983. Regulation: 8.