ULTRA-VU ANGIOSCOPE

ULTRA-VU ANGIOSCOPE is an FDA 510(k)-cleared medical device (K902329) manufactured by Angiolaz, Inc.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 21, 1990. Regulation: 8.