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Cliniqa Corporation
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LINICAL PROTEIN 3 CALIBRATION VERIFIERS LEVELS A - E FOR THE BECKMAN-COULTER IMMAGE is an FDA 510(k)-cleared medical device (K022867) 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 1, 2002. Regulation: 8.