Diazyme Receives FDA 510(k) Clearance for HDL-Cholesterol Assay

Mar 06, 2008

POWAY, CA - March 6, 2008 -- Diazyme Laboratories announced today that the U.S. Food and Drug Administration (FDA) has granted Diazyme 510(k) clearance to market its HDL-Cholesterol Assay Kit for the quantitative determination of High Density Lipoprotein Cholesterol in human serum or plasma. Diazyme uses a modified PVS and PEGME coupled classic precipitation method. This homogeneous two reagent system requires no sample pre-treatment and is cost effective and liquid stable. The method is not interfered by triglyceride up to 1000 mg/dL, hemoglobin up to 1,000 mg/dL, bilirubin up to 30 mg/dL and ascorbic acid up to 176 mg/dL. The assay features an extended linear range from 1.06 mg/dL to 184 mg/dL, has minimal sample size requirement of only 3 ?L and is readily adaptable to automated chemistry instrumentation.

Diazyme Laboratories uses its platform technologies to develop low cost and uniform diagnostic products for clinical and research use. Products include diagnostic blood tests for liver disease, cardiac markers, diabetes, renal disease and electrolytes. Diazyme's enzyme technology and related products can be found on its website at www.diazyme.com.

For further information contact:

Diazyme Laboratories:
Chong Yuan
(858) 455-4760

Public Relations:
Doug Fouquet
(858) 455-2173