
Fujifilm Medical Systems U.S.A, Inc.
Free shipping on orders over $99 · 30-day returns
FUJIFILM 600 SERIES ENDOSCOPES is an FDA 510(k)-cleared medical device (K132210) manufactured by Fujifilm Medical Systems U.S.A, 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 January 9, 2014. Regulation: 8.