ALOKA MODEL SSD-650 ULTRASOUND IMAGING SYSTEM

ALOKA MODEL SSD-650 ULTRASOUND IMAGING SYSTEM is an FDA 510(k)-cleared medical device (K895449) manufactured by Ge Medical Systems Information Technologies. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 4, 1990. Regulation: 8.