P-2 ULTRASONIC ARTERIOGRAPH

P-2 ULTRASONIC ARTERIOGRAPH is an FDA 510(k)-cleared medical device (K792015) manufactured by D. E. Hokanson, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 3, 1979. Regulation: 8.