
DiaSorin, Inc.
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LIAISON® EA IgG and LIAISON® EA IgG Serum Control Set is an FDA 510(k)-cleared medical device (K162959) manufactured by DiaSorin, Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on January 3, 2017. Regulation: 8.

ADC
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