Roche Reagent for Alt

FDA 510(k) K924245 · Roche Diagnostic Systems, Inc.

Substantially Equivalent

510(k) numberK924245

Submission

Device name
Roche Reagent for Alt
Applicant
Roche Diagnostic Systems, Inc.
Branchburg, NJ, US
Received
August 24, 1992
Decision date
October 22, 1992
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
CKA – Nadh Oxidation/Nad Reduction, Alt/Sgpt
Device class
Class I (low risk)
Regulation
21 CFR 862.1030
Specialty
Clinical Chemistry

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K113382Ace Alt ReagentCKA · Traditional Alfa Wassermann07/19/2012SE
K061020Dimension Vista Albumin, Alkaline Phosphatase, Aspartate Amino Transferase…CKA · Special Dade Behring, Inc.05/10/2006SE
K020487Careside AltCKA · Traditional Careside, Inc.06/04/2002SE
K980028Alt (GPT) Liquid Stable 2 Vial - Incorporating Dynamic Stabilization Technology - (DST)CKA · Traditional Trace America, Inc.02/02/1998SE
K973869Trace Reagent Line for the Cobas MiraCKA · Traditional Trace America, Inc.01/07/1998SE
K974003Alanine Aminotransferase-Sl Assay Catalogue Number 318-10, 318-30CKA · Traditional Diagnostic Chemicals , Ltd.12/05/1997SE
K971323Alt or SGPTCKA · Traditional Carolina Liquid Chemistries Corp.04/21/1997SE
K965134Alt/SgptCKA · Traditional Derma Media Lab., Inc.02/18/1997SE
K961123Alt Incorporating DSTCKA · Traditional Trace Scientific , Ltd.04/25/1996SE

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Questions and answers

When was Roche Reagent for Alt cleared by the FDA?

Roche Reagent for Alt (K924245) received a 510(k) decision of Substantially Equivalent on October 22, 1992, 59 days after the submission was received.

What is the product code of K924245?

The FDA product code is CKA – Nadh Oxidation/Nad Reduction, Alt/Sgpt, a Class I (low risk) device regulated under 21 CFR 862.1030.