FIBER OPTIC ENDOILLUMINATION PROBE

FIBER OPTIC ENDOILLUMINATION PROBE is an FDA 510(k)-cleared medical device (K980636) manufactured by Dutch Ophthalmic 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 May 19, 1998. Regulation: 8.