
Kent Laboratories, Inc.
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RADIAL IMMUNO-TEST FOR HUMAN C-REACTI is an FDA 510(k)-cleared medical device (K831958) 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 18, 1983. Regulation: 8.