VISITEC NEEDLE RANGE (GENERAL HOSPITAL)

VISITEC NEEDLE RANGE (GENERAL HOSPITAL) is an FDA 510(k)-cleared medical device (K811966) manufactured by Visitec Co.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 22, 1981. Regulation: 8.