Urinary Free Catecholamines & Metanephrines (HPLC)

FDA 510(k) K873371 · Bio-Rad

Substantially Equivalent

510(k) numberK873371

Submission

Device name
Urinary Free Catecholamines & Metanephrines (HPLC)
Applicant
Bio-Rad
Hercules, CA, US
Received
August 21, 1987
Decision date
January 5, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CHQ – Chromatographic/Fluorometric Method, Catecholamines
Device class
Class I (low risk)
Regulation
21 CFR 862.1165
Specialty
Clinical Chemistry

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K032199Esa Plasma Free Metanephrine Analysis KitCHQ · Traditional Esa, Inc.01/30/2004SE
K972167Plasma Catecholamine KitCHQ · Traditional Bioanalytical Systems, Inc.08/04/1997SE
K963938Model 5500 CeasCHQ · Traditional Esa, Inc.12/26/1996SE
K952919Urinary Metanephrine KitCHQ · Traditional Bioanalytical Systems, Inc.09/06/1995SE
K943099Urinary Catecholamine KitCHQ · Traditional Bioanalytical Systems, Inc.10/07/1994SE
K931148Model 5500 Coulochem Electrode Array SystemCHQ · Traditional Esa, Inc.06/09/1993SE
K894966Plasma Catecholamines by HPLCCHQ · Traditional Bio-Rad10/25/1989SE
K855214CAT-3 Catecholamine Assay KitCHQ · Traditional Whale Scientific, Inc.03/14/1986SE

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Questions and answers

When was Urinary Free Catecholamines & Metanephrines (HPLC) cleared by the FDA?

Urinary Free Catecholamines & Metanephrines (HPLC) (K873371) received a 510(k) decision of Substantially Equivalent on January 5, 1988, 137 days after the submission was received.

What is the product code of K873371?

The FDA product code is CHQ – Chromatographic/Fluorometric Method, Catecholamines, a Class I (low risk) device regulated under 21 CFR 862.1165.