Supelco, Inc.
IN VITRO DIAGNOSTIC STANDARDS
SKU K802278UPC DIF
In Stock
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IFDA 510(k) Cleared (K802278)
1
Free shipping on orders over $99 · 30-day returns
Supelco, Inc.
Free shipping on orders over $99 · 30-day returns
IN VITRO DIAGNOSTIC STANDARDS is an FDA 510(k)-cleared medical device (K802278) manufactured by Supelco, Inc.. This device is classified under the Clinical Toxicology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on November 23, 1980. Regulation: 8.
