Diazyme Introduces New Test for the Early Detection of Kidney Disease
POWAY, CA - Diazyme Laboratories announced today that the U.S. Food and Drug Administration (FDA) has granted Diazyme 510(k) clearance to market its Cystatin C Assay Kit for the quantitative determination of Cystatin C in serum and plasma samples. Cystatin C is emerging as a biomarker superior to standard tests of kidney function in the early detection of chronic kidney disease. There is a growing body of evidence that indicates that some of the negative outcomes of chronic kidney disease can be averted with early diagnosis and treatment.
The Diazyme method is a liquid stable, two reagent immunoturbidmeteric system which can be applied to most common clinical chemistry instrumentation. Diazyme has developed an extensive listing of instrument parameters and, along with multiple packaging formats, offers the added convenience of instrument specific formats suitable for use in laboratories of all volumes and workflows.
The assay features excellent accuracy and precision and offers an extended reportable range of 0.47 to over 8 mg/L which will reduce the need for re-testing elevated patient samples. The method also demonstrates insignificant bias from interferents commonly found in serum including highly elevated levels of hemoglobin, bilirubin, triglycerides and ascorbic acid.
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