Glucose Oxidase Enzymatic Reagent Set

FDA 510(k) K843528 · Livonia Diagnostics, Inc.

Substantially Equivalent

510(k) numberK843528

Submission

Device name
Glucose Oxidase Enzymatic Reagent Set
Applicant
Livonia Diagnostics, Inc.
Walker, MI, US
Received
September 7, 1984
Decision date
September 28, 1984
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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Questions and answers

When was Glucose Oxidase Enzymatic Reagent Set cleared by the FDA?

Glucose Oxidase Enzymatic Reagent Set (K843528) received a 510(k) decision of Substantially Equivalent on September 28, 1984, 21 days after the submission was received.

What is the product code of K843528?

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