
U. S. Diagnostics, Inc.
Free shipping on orders over $99 · 30-day returns
U.S. DIAGNOSTICS LIQUID LD ISOENZYME CONTROL is an FDA 510(k)-cleared medical device (K870737) manufactured by U. S. Diagnostics, Inc.. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 12, 1987. Regulation: 8.