Quantimune Cortisol Ria Cortisol Radio-

FDA 510(k) K800045 · Bio-Rad

Substantially Equivalent

510(k) numberK800045

Submission

Device name
Quantimune Cortisol Ria Cortisol Radio-
Applicant
Bio-Rad
Mchenry, IL, US
Received
January 8, 1980
Decision date
January 23, 1980
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CGR – Radioimmunoassay, Cortisol
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1205
Specialty
Clinical Chemistry

Other 510(k)s with product code CGR

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K242190Access Cortisol; DxC 500i Clinical AnalyzerCGR · Traditional Beckman Coulter, Inc.03/05/2025SE
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K202136IDS CortisolCGR · Traditional Immunodiagnostic Systems , Ltd.04/13/2021SE
K203270IMMULITE/IMMULITE® 1000 CortisolCGR · Traditional Siemens Healthcare Diagnostics Products, Ltd.01/15/2021SE
K202826IMMULITE® 2000 CortisolCGR · Traditional Siemens Healthcare Diagnostics Products, Ltd.01/15/2021SE
K062626Cortisol ElisaCGR · Traditional Ibl-Hamburg GmbH12/20/2006SE
K060480Vitros Immunodiagnostic Products Cortisol Reagent Pack and Calibrators and Metabolism…CGR · Traditional Ortho-Clinical Diagnostics07/03/2006SE
K052359Ibl Cortisol Lia Test KitCGR · Traditional Lehnus & Associates Consulting10/03/2005SE
K050202Cortisol and Cortisol Calibrators on the Access Immunoassay SystemsCGR · Special Beckman Coulter, Inc.02/09/2005SE
K042689Nichols Advantage CortisolCGR · Traditional Nichols Institute Diagnostics12/09/2004SE

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Questions and answers

When was Quantimune Cortisol Ria Cortisol Radio- cleared by the FDA?

Quantimune Cortisol Ria Cortisol Radio- (K800045) received a 510(k) decision of Substantially Equivalent on January 23, 1980, 15 days after the submission was received.

What is the product code of K800045?

The FDA product code is CGR – Radioimmunoassay, Cortisol, a Class II (moderate risk) device regulated under 21 CFR 862.1205.