
J.S. Medical Assoc.
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ACCUTEX RHEUMATIOD FACTOR (RF) LATEX TEST is an FDA 510(k)-cleared medical device (K924036) manufactured by J.S. Medical Assoc.. 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 30, 1992. Regulation: 8.