TRIPPI-WELLS DUAL PURPOSE UNIVERSAL TONG

TRIPPI-WELLS DUAL PURPOSE UNIVERSAL TONG is an FDA 510(k)-cleared medical device (K810193) manufactured by Ace Orthopedic Manufacturing Co.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 19, 1981. Regulation: 8.