FIBER OPTIC LIGHT GUIDE CAT#60-0768

FIBER OPTIC LIGHT GUIDE CAT#60-0768 is an FDA 510(k)-cleared medical device (K802767) manufactured by Aspen Laboratories, Inc.. This device is classified under the Ear, Nose, Throat specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on December 15, 1980. Regulation: 8.