
Cliniqa Corporation
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CLINIQA LIQUIDQC IMMUNOASSAY CONTROL LEVEL 1, 2 & 3 is an FDA 510(k)-cleared medical device (K083554) manufactured by Cliniqa Corporation. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 20, 2009. Regulation: 8.