ALOKA 650CL DIAGNOSTIC ULTRASOUND SYSTEM

ALOKA 650CL DIAGNOSTIC ULTRASOUND SYSTEM is an FDA 510(k)-cleared medical device (K920374) manufactured by Ge Medical Systems Information Technologies. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 1, 1992. Regulation: 8.