
Tosoh Medics, Inc.
Free shipping on orders over $99 · 30-day returns
AIA NEXIA-AUTOMATED ENZYME IMMUNOASSAY SYSTEM is an FDA 510(k)-cleared medical device (K971103) manufactured by Tosoh Medics, Inc.. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on June 26, 1997. Regulation: 8.