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Bio-Rad, Diagnostics Grp.
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LIQUICHEK URINALYSIS CONTROL (BI-LEVEL), CONTROL LEVEL1, LEVEL 2,MINIPAK, 435,436,437,435X is an FDA 510(k)-cleared medical device (K070848) manufactured by Bio-Rad, Diagnostics Grp.. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 24, 2007. Regulation: 8.