Hybritech, Inc.
TANDEM-E IGE II CALIBRATION VERIFICATION SET
SKU K922754UPC JJX
In Stock
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IFDA 510(k) Cleared (K922754)
1
Free shipping on orders over $99 · 30-day returns
Hybritech, Inc.
Free shipping on orders over $99 · 30-day returns
TANDEM-E IGE II CALIBRATION VERIFICATION SET is an FDA 510(k)-cleared medical device (K922754) manufactured by Hybritech, Inc.. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on February 16, 1993. Regulation: 8.
