Kodak Ektachem Clinical Chemistry Slide for Asparate Amimotransferase

FDA 510(k) K934413 · Eastman Kodak Company

Substantially Equivalent

510(k) numberK934413

Submission

Device name
Kodak Ektachem Clinical Chemistry Slide for Asparate Amimotransferase
Applicant
Eastman Kodak Company
Rochester, NY, US
Received
September 10, 1993
Decision date
April 25, 1994
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
CIT – Nadh Oxidation/Nad Reduction, Ast/Sgot
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1100
Specialty
Clinical Chemistry

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K023551Wiener Lab Got (Ast) UV Aa LiquidaCIT · Traditional Wiener Laboratories Saic12/09/2002SE
K013698Ast (Sgot)CIT · Traditional Jas Diagnostics, Inc.12/21/2001SE
K013145Wiener Lab. Got (Ast) UV Aa. Weiner Lab. Got (Ast) UV Unitest, Models 10 * 20 ML Cat.…CIT · Traditional Wiener Laboratories Saic11/27/2001SE
K010488Atac Pak Ast Reagent KitCIT · Traditional Elan Holdings, Inc.04/09/2001SE

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Questions and answers

When was Kodak Ektachem Clinical Chemistry Slide for Asparate Amimotransferase cleared by the FDA?

Kodak Ektachem Clinical Chemistry Slide for Asparate Amimotransferase (K934413) received a 510(k) decision of Substantially Equivalent on April 25, 1994, 227 days after the submission was received.

What is the product code of K934413?

The FDA product code is CIT – Nadh Oxidation/Nad Reduction, Ast/Sgot, a Class II (moderate risk) device regulated under 21 CFR 862.1100.