JUMBO DIGITAL GAMMACAMERA GCA-90B WI & W2

JUMBO DIGITAL GAMMACAMERA GCA-90B WI & W2 is an FDA 510(k)-cleared medical device (K853470) manufactured by Toshiba Medical Systems. This device is classified under the Radiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on November 18, 1985. Regulation: 8.