Quidel Corporation
SOFIA STREP A FIA
SKU K123793UPC GTY
In Stock
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IFDA 510(k) Cleared (K123793)
1
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Quidel Corporation
Free shipping on orders over $99 · 30-day returns
SOFIA STREP A FIA is an FDA 510(k)-cleared medical device (K123793) manufactured by Quidel Corporation. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on June 16, 2013. Regulation: 8.
