V.I. OCTOSON ULTRASONIC SYSTEM

V.I. OCTOSON ULTRASONIC SYSTEM is an FDA 510(k)-cleared medical device (K760874) manufactured by General Electric Co.. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 15, 1976. Regulation: 8.