ALOKA PROUSOUND F75 DIAGNOSTIC ULTRASOUND SYSTEM

ALOKA PROUSOUND F75 DIAGNOSTIC ULTRASOUND SYSTEM is an FDA 510(k)-cleared medical device (K110207) 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 16, 2011. Regulation: 8.