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9/2/2010
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Quidel's RapidVue hCG lateral flow pregnancy immunoassay granted FDA 510(k) clearance
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Quidel Corporation, a leading service provider of rapid diagnostic testing solutions, announced today that it has recognized 510(k) clearance from the United States Food and Drug supervision (FDA) for the sale of Quidel's RapidVue® hCG test, a lateral flow germination immunoassay for the qualitative disclosure of human Chorionic Gonadotropin (hCG). More: - The rest... |
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