Coritsol Premix Ria Kit

FDA 510(k) K842957 · Biotecx Laboratories, Inc.

Substantially Equivalent

510(k) numberK842957

Submission

Device name
Coritsol Premix Ria Kit
Applicant
Biotecx Laboratories, Inc.
Mchenry, IL, US
Received
July 27, 1984
Decision date
September 14, 1984
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

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K042689Nichols Advantage CortisolCGR · Traditional Nichols Institute Diagnostics12/09/2004SE

More from Nichols Institute Diagnostics

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K893620T3 Clasp-Bead Eia KitCDP · Traditional 08/11/1989SE
K892853T4 Clasp-Bead Eia KitKLI · Traditional 05/22/1989SE
K883765TBG 125I Ria Kit, Radioimmuno. of Serum ThyroxineKHQ · Traditional 10/31/1988SE
K871211Progesterone Clasp Radioimmunoassay KitJLS · Traditional 04/13/1987SE
K863188HPL Ria KitJMX · Traditional 09/25/1986SE
K854876Aldosterone Direct Ria KitKQN · Traditional 03/17/1986SE
K851540Estradiol Direct Ria KitCHP · Traditional 06/06/1985SE

Questions and answers

When was Coritsol Premix Ria Kit cleared by the FDA?

Coritsol Premix Ria Kit (K842957) received a 510(k) decision of Substantially Equivalent on September 14, 1984, 49 days after the submission was received.

What is the product code of K842957?

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