Enzymatic Urea Nitrogen Reagent Set

FDA 510(k) K860109 · Technostics Intl.

Substantially Equivalent

510(k) numberK860109

Submission

Device name
Enzymatic Urea Nitrogen Reagent Set
Applicant
Technostics Intl.
Washington, MI, US
Received
January 13, 1986
Decision date
February 6, 1986
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.

510(k)DeviceDecision
K855188CPK (UV) Reagent KitJHS · Traditional 03/05/1986SE
K860111Uric Acid Reagent SetLFQ · Traditional 02/19/1986SE
K855190Magnesium Reagent SetJGJ · Traditional 02/18/1986SE
K860110Glutamic Pyruvic Transaminase, Gpt(Uv) Reagent SetCKA · Traditional 02/11/1986SE
K860112Total Lipids Reagent SetCFD · Traditional 01/24/1986SE
K855185Glucose Reagent SetCGE · Traditional 01/22/1986SE
K855157Lactic Dehydrogenase (VV) Reagent SetCFJ · Traditional 01/21/1986SE
K855195Direct & Total Bilirubin SetCIG · Traditional 01/14/1986SE
K855194Glucose Oxidase Reagent SetCGA · Traditional 01/14/1986SE
K855193Creatinine Reagent SetCGX · Traditional 01/14/1986SE

Questions and answers

When was Enzymatic Urea Nitrogen Reagent Set cleared by the FDA?

Enzymatic Urea Nitrogen Reagent Set (K860109) received a 510(k) decision of Substantially Equivalent on February 6, 1986, 24 days after the submission was received.

What is the product code of K860109?

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