MICROVISION FAST DETAIL INTENSIFYING SCREEN

MICROVISION FAST DETAIL INTENSIFYING SCREEN is an FDA 510(k)-cleared medical device (K931283) 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 June 7, 1993. Regulation: 8.