Urea Nitrogen (Bun)

FDA 510(k) K880078 · Tech-Neal Scientific, Inc.

Substantially Equivalent

510(k) numberK880078

Submission

Device name
Urea Nitrogen (Bun)
Applicant
Tech-Neal Scientific, Inc.
Westmont, IL, US
Received
January 11, 1988
Decision date
February 11, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CDQ – Urease And Glutamic Dehydrogenase, Urea Nitrogen
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1770
Specialty
Clinical Chemistry

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More from Hemagen Diagnostics, Inc.

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K882256Magnesium Reagent SetJGJ · Traditional 08/08/1988SE
K882459Diazo, Colorimetric BilirubinCIG · Traditional 08/02/1988SE
K881239Gamma Glutamyl Transferase Reagent SetJPZ · Traditional 05/31/1988SE
K881241Total Bilirubin ReagentCIG · Traditional 05/27/1988SE
K881240Chloride Reagent SetCHJ · Traditional 04/28/1988SE
K881237Creatine Kinase (CK) Reagent SetJHX · Traditional 04/28/1988SE
K880237CholesterolCHH · Traditional 04/28/1988SE
K880277Uric Acid Reagent SetKNK · Traditional 04/18/1988SE
K880845Calcium Reagent SetCIC · Traditional 04/05/1988SE
K880844Albumin Reagent SetCIX · Traditional 04/05/1988SE

Questions and answers

When was Urea Nitrogen (Bun) cleared by the FDA?

Urea Nitrogen (Bun) (K880078) received a 510(k) decision of Substantially Equivalent on February 11, 1988, 31 days after the submission was received.

What is the product code of K880078?

The FDA product code is CDQ – Urease And Glutamic Dehydrogenase, Urea Nitrogen, a Class II (moderate risk) device regulated under 21 CFR 862.1770.