
Cliniqa Corporation
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CLINIQA LIQUID QC CARDIAC MARKER CONTROL SP, LEVELS 1,2, &3 is an FDA 510(k)-cleared medical device (K062916) 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 October 22, 2006. Regulation: 8.