Hepatic Enzymes on Abx Pentra 400 Clinical Chemistry Analyzer

FDA 510(k) K060318 · Horiba Abx

Substantially Equivalent

510(k) numberK060318

Submission

Device name
Hepatic Enzymes on Abx Pentra 400 Clinical Chemistry Analyzer
Applicant
Horiba Abx
Montpellier, FR
Received
February 8, 2006
Decision date
August 8, 2006
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary 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
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K010488Atac Pak Ast Reagent KitCIT · Traditional Elan Holdings, Inc.04/09/2001SE
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Questions and answers

When was Hepatic Enzymes on Abx Pentra 400 Clinical Chemistry Analyzer cleared by the FDA?

Hepatic Enzymes on Abx Pentra 400 Clinical Chemistry Analyzer (K060318) received a 510(k) decision of Substantially Equivalent on August 8, 2006, 181 days after the submission was received.

What is the product code of K060318?

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