
Fujinon, Inc.
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200 SERIES GASTRO-INTESTINAL VIDEO SYSTEM is an FDA 510(k)-cleared medical device (K944759) manufactured by Fujinon, 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 April 10, 1995. Regulation: 8.