DETERM. SIZE 72 RADIAL-HUMAN IGD

DETERM. SIZE 72 RADIAL-HUMAN IGD is an FDA 510(k)-cleared medical device (K831956) manufactured by Kent Laboratories, Inc.. This device is classified under the Immunology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 17, 1983. Regulation: 8.