July 15–19, 2012

May 25, 2011
Diazyme Receives 510(k) FDA Approval for Enzymatic Glycated Serum Protein (Glycated Albumin) Assay Kit

Jan 24, 2011
Diazyme Receives FDA 510(k) Clearance for Vitamin D Assay

May 07, 2010
Diazyme Receives FDA 510(k) Clearance to Market SMART HbA1c Assay on Its SMART Point of Care System for Diabetes Monitoring

Jul 20, 2009
Diazyme homocysteine Test Receives AACC Award

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Products by Medical Condition

Diazyme uses its proprietary enzyme technologies to develop diagnostic reagents which can be used on most automated chemistry analyzers in user-friendly formats. Diazyme’s products include test kits for diagnosis of cardiovascular disease, liver disease, cancer markers, renal disease, and electrolytes.

Diazyme Laboratories is a Division of General Atomics located in Poway, California and is a cGMP and ISO 13485 certified medical device manufacturer.