CAMSYS 6300

CAMSYS 6300 is an FDA 510(k)-cleared medical device (K920574) manufactured by F.M. Wiest USA, 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 February 16, 1993. Regulation: 8.