Glucose Oxidase Reagent Set

FDA 510(k) K855194 · Technostics Intl.

Substantially Equivalent

510(k) numberK855194

Submission

Device name
Glucose Oxidase Reagent Set
Applicant
Technostics Intl.
Washington, MI, US
Received
December 26, 1985
Decision date
January 14, 1986
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CGA – Glucose Oxidase, Glucose
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1345
Specialty
Clinical Chemistry

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More from Nova Biomedical Corporation

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K860110Glutamic Pyruvic Transaminase, Gpt(Uv) Reagent SetCKA · Traditional 02/11/1986SE
K860109Enzymatic Urea Nitrogen Reagent SetCDQ · Traditional 02/06/1986SE
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
K855193Creatinine Reagent SetCGX · Traditional 01/14/1986SE

Questions and answers

When was Glucose Oxidase Reagent Set cleared by the FDA?

Glucose Oxidase Reagent Set (K855194) received a 510(k) decision of Substantially Equivalent on January 14, 1986, 19 days after the submission was received.

What is the product code of K855194?

The FDA product code is CGA – Glucose Oxidase, Glucose, a Class II (moderate risk) device regulated under 21 CFR 862.1345.