Sri(Tm) Cortisol Enzyme Immunoassay(Mag Sol Phase)

FDA 510(k) K914886 · Serono-Baker Diagnostics, Inc.

Substantially Equivalent

510(k) numberK914886

Submission

Device name
Sri(Tm) Cortisol Enzyme Immunoassay(Mag Sol Phase)
Applicant
Serono-Baker Diagnostics, Inc.
Allentown, PA, US
Received
October 30, 1991
Decision date
March 2, 1992
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

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

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Questions and answers

When was Sri(Tm) Cortisol Enzyme Immunoassay(Mag Sol Phase) cleared by the FDA?

Sri(Tm) Cortisol Enzyme Immunoassay(Mag Sol Phase) (K914886) received a 510(k) decision of Substantially Equivalent on March 2, 1992, 124 days after the submission was received.

What is the product code of K914886?

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