ALOKA 680 DIAGNOSTIC ULTRASOUND SCANNING SYSTEM

ALOKA 680 DIAGNOSTIC ULTRASOUND SCANNING SYSTEM is an FDA 510(k)-cleared medical device (K896755) 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 May 6, 1990. Regulation: 8.