Ultra-Violet Bun Reagent Kit (Rate)

FDA 510(k) K871547 · Biochemical Trade, Inc.

Substantially Equivalent

510(k) numberK871547

Submission

Device name
Ultra-Violet Bun Reagent Kit (Rate)
Applicant
Biochemical Trade, Inc.
Miami, FL, US
Received
April 20, 1987
Decision date
June 22, 1987
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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K910296Phosphorus (Inorganic) Test SystemCEO · Traditional 02/27/1991SE
K905776Albumin Reagent SetCJW · Traditional 02/26/1991SE
K905790Total Protein Reagent SetCEK · Traditional 02/21/1991SE
K905650Kinetic Alkaline Phosphatase DeterminationCJE · Traditional 02/13/1991SE
K905619Creatinine (Rate) Reagent SetCGX · Traditional 02/13/1991SE
K905651Kinetic Amylase DeterminationJFJ · Traditional 01/31/1991SE
K905649Gamma-Glutamyl Transferase DeterminationJQB · Traditional 01/30/1991SE
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Questions and answers

When was Ultra-Violet Bun Reagent Kit (Rate) cleared by the FDA?

Ultra-Violet Bun Reagent Kit (Rate) (K871547) received a 510(k) decision of Substantially Equivalent on June 22, 1987, 63 days after the submission was received.

What is the product code of K871547?

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