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Roche Diagnostics
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TINA-QUANT ALBUMIN GEN 2 is an FDA 510(k)-cleared medical device (K101203) manufactured by Roche Diagnostics. This device is classified under the Immunology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 9, 2010. Regulation: 8.