VISITEC NEEDLE RANGE (ANESTHESIOLOGY)

VISITEC NEEDLE RANGE (ANESTHESIOLOGY) is an FDA 510(k)-cleared medical device (K811963) manufactured by Visitec Co.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 15, 1981. Regulation: 8.