Cortisol Reagent System

FDA 510(k) K760939 · Beckman Instruments, Inc.

Substantially Equivalent

510(k) numberK760939

Submission

Device name
Cortisol Reagent System
Applicant
Beckman Instruments, Inc.
Mchenry, IL, US
Received
November 1, 1976
Decision date
November 16, 1976
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

510(k)DeviceApplicantDecision
K242190Access Cortisol; DxC 500i Clinical AnalyzerCGR · Traditional Beckman Coulter, Inc.03/05/2025SE
K223038Access CortisolCGR · Traditional Beckman Coulter, Inc.02/08/2023SE
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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K980173Access Total BHCG Reagents on the Access Immunoassay Analyzer; 33500, 33505JHI · Traditional 03/18/1998SE
K974816Access(R) Psa Reagents on the Access(R) Immunoassay Analyzer 33220, 33225, 33229LTJ · Traditional 02/20/1998SE
K974564Immage Immunochemistry System ALPHA-2-MACROGLOBULIN ReagentDEB · Traditional 02/17/1998SE
K974110Immage Immunochemistry System Antithrombin III (AT3) ReagentJBQ · Traditional 12/24/1997SE
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Questions and answers

When was Cortisol Reagent System cleared by the FDA?

Cortisol Reagent System (K760939) received a 510(k) decision of Substantially Equivalent on November 16, 1976, 15 days after the submission was received.

What is the product code of K760939?

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