Enzymun Test(R) Cortisol

FDA 510(k) K900485 · Boehringer Mannheim Corp.

Substantially Equivalent

510(k) numberK900485

Submission

Device name
Enzymun Test(R) Cortisol
Applicant
Boehringer Mannheim Corp.
Indianapolis, IN, US
Received
February 1, 1990
Decision date
May 2, 1990
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

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Questions and answers

When was Enzymun Test(R) Cortisol cleared by the FDA?

Enzymun Test(R) Cortisol (K900485) received a 510(k) decision of Substantially Equivalent on May 2, 1990, 90 days after the submission was received.

What is the product code of K900485?

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