SSD-633 PHASED ARRAY SECTOR/LINEAR ULTRASOUND SYS.

SSD-633 PHASED ARRAY SECTOR/LINEAR ULTRASOUND SYS. is an FDA 510(k)-cleared medical device (K870916) manufactured by Ge Medical Systems Information Technologies. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 20, 1987. Regulation: 8.