
International Enzymes, Inc.
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LINICAL PROTEIN I CALIBRATION VERIFIERS LEVELS A - FOR BECKMAN ARRAY 360 SYSTEM is an FDA 510(k)-cleared medical device (K950802) manufactured by International Enzymes, Inc.. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on May 31, 1995. Regulation: 8.