SPECULUM, VAGINAL, METAL FIBEROPTIC

SPECULUM, VAGINAL, METAL FIBEROPTIC is an FDA 510(k)-cleared medical device (K864865) manufactured by Luxtec Corp.. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on January 8, 1987. Regulation: 8.