ACKRAD N-DO VAGE TUBE

ACKRAD N-DO VAGE TUBE is an FDA 510(k)-cleared medical device (K813607) manufactured by Ackrad Laboratories. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 4, 1982. Regulation: 8.