
Kent Laboratories, Inc.
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72 DETERM. SIZE RADIAL IMMUNO. TEST HUMAN CERULOPL is an FDA 510(k)-cleared medical device (K850682) 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 November 24, 1985. Regulation: 8.