ALOKA SSD-2000 DIAGNOSTIC ULTRASOUND SYSTEM MODIFICATION

ALOKA SSD-2000 DIAGNOSTIC ULTRASOUND SYSTEM MODIFICATION is an FDA 510(k)-cleared medical device (K941652) manufactured by Aloka Co., Ltd.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 20, 1994. Regulation: 8.