INTERSOURCE 125, MODEL 1251L

INTERSOURCE 125, MODEL 1251L is an FDA 510(k)-cleared medical device (K984235) manufactured by International Brachytherapy, Inc.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 8, 1999. Regulation: 8.