SYSTEM, ECHO, PULSED ULTRASONIC DIAG.

SYSTEM, ECHO, PULSED ULTRASONIC DIAG. is an FDA 510(k)-cleared medical device (K802708) manufactured by General Electric Co.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 6, 1981. Regulation: 8.