SSD-2000 DIAG. ULTRASOUND SYS.&UST-979-3.5 TRANS.

SSD-2000 DIAG. ULTRASOUND SYS.&UST-979-3.5 TRANS. is an FDA 510(k)-cleared medical device (K925646) 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 February 11, 1993. Regulation: 8.