MEDIGROUP LG-102 LIGHT GUIDE

MEDIGROUP LG-102 LIGHT GUIDE is an FDA 510(k)-cleared medical device (K823293) manufactured by Medigroup. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 4, 1983. Regulation: 8.