ULTRA-VISION RAPID INTENSIFYING SCREEN

ULTRA-VISION RAPID INTENSIFYING SCREEN is an FDA 510(k)-cleared medical device (K920190) 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 May 27, 1992. Regulation: 8.