
Trinity Laboratories, Inc.
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RHEUMA-LEX(TM) SYST: RHEUMATOID FACTOR LATEX TEST is an FDA 510(k)-cleared medical device (K915320) manufactured by Trinity 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 December 6, 1992. Regulation: 8.