
Bayer Diagnostics Corp.
Free shipping on orders over $99 · 30-day returns
AMMONIA ASSAY FOR THE ADVIA INTEGRATED MODULAR SYSTEM is an FDA 510(k)-cleared medical device (K021151) manufactured by Bayer Diagnostics Corp.. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on July 12, 2002. Regulation: 8.