CRONEX QUANTA III INTENSIFYING SCREENS

CRONEX QUANTA III INTENSIFYING SCREENS is an FDA 510(k)-cleared medical device (K770574) manufactured by E.I. Dupont DE Nemours & Co., Inc.. This device is classified under the Radiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 4, 1977. Regulation: 8.