IMMUNODIP URINARY ALBUMIN SCREEN ASSAY, CATALOGUE NUMBER 790-25

IMMUNODIP URINARY ALBUMIN SCREEN ASSAY, CATALOGUE NUMBER 790-25 is an FDA 510(k)-cleared medical device (K022538) manufactured by Diagnostic Chemicals, Ltd. (Usa). This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on August 22, 2002. Regulation: 8.