Ast/Sgot Liquid Reagent - Kinetic Method

FDA 510(k) K981650 · Teco Diagnostics

Substantially Equivalent

510(k) numberK981650

Submission

Device name
Ast/Sgot Liquid Reagent - Kinetic Method
Applicant
Teco Diagnostics
Anaheim, CA, US
Received
May 11, 1998
Decision date
June 29, 1998
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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K071525Activated Aspartate AminotransferaseCIT · Traditional Abbott Laboratories03/19/2008SE
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K071211Cobas C 111 AnalyzerCIT · Traditional Roche Diagnostics07/30/2007SE
K060318Hepatic Enzymes on Abx Pentra 400 Clinical Chemistry AnalyzerCIT · Traditional Horiba Abx08/08/2006SE
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 Ast/Sgot Liquid Reagent - Kinetic Method cleared by the FDA?

Ast/Sgot Liquid Reagent - Kinetic Method (K981650) received a 510(k) decision of Substantially Equivalent on June 29, 1998, 49 days after the submission was received.

What is the product code of K981650?

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