Access Cortisol Reagents

FDA 510(k) K940221 · Bio-Rad Laboratories, Inc.

Substantially Equivalent

510(k) numberK940221

Submission

Device name
Access Cortisol Reagents
Applicant
Bio-Rad Laboratories, Inc.
Chaska, MN, US
Received
January 18, 1994
Decision date
April 26, 1994
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

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
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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Questions and answers

When was Access Cortisol Reagents cleared by the FDA?

Access Cortisol Reagents (K940221) received a 510(k) decision of Substantially Equivalent on April 26, 1994, 98 days after the submission was received.

What is the product code of K940221?

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