MAXICAMERA 400T W/BODY CONTOUR TOMOGRA

MAXICAMERA 400T W/BODY CONTOUR TOMOGRA is an FDA 510(k)-cleared medical device (K841996) manufactured by General Electric Co.. This device is classified under the Radiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on July 15, 1984. Regulation: 8.