P-1 ULTRASONIC ARTERIOGRAPH

P-1 ULTRASONIC ARTERIOGRAPH is an FDA 510(k)-cleared medical device (K761288) manufactured by D. Eugene Hokanson. 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 27, 1976. Regulation: 8.