Olympus Cholinesterase Reagent (Catalog Number OSR6114)

FDA 510(k) K030045 · Olympus America, Inc.

Substantially Equivalent

510(k) numberK030045

Submission

Device name
Olympus Cholinesterase Reagent (Catalog Number OSR6114)
Applicant
Olympus America, Inc.
Irving, TX, US
Received
January 6, 2003
Decision date
February 21, 2003
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
DIH – Colorimetry, Cholinesterase
Device class
Class I (low risk)
Regulation
21 CFR 862.3240
Specialty
Clinical Toxicology

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K103373Synchron Systems Cholinesterase (Chex) Model A53722DIH · Traditional Beckman Coulter, Inc.02/07/2011SE
K061093Cholinesterase GEN.2 Test SystemDIH · Traditional Roche Diagnostics Corp.07/03/2006SE
K051444Sentinel Cholinesterase LiquidDIH · Special Sentinel Ch. Srl06/20/2005SE
K023992Wiener Lab Colinesterasa AaDIH · Traditional Wiener Laboratories Saic02/12/2003SE
K013750Advia 1650 Cholinesterase AssayDIH · Traditional Bayer Diagnostics Corp.01/18/2002SE
K002792Careside CholinesteraseDIH · Traditional Careside, Inc.11/08/2000SE
K001344Advia ImsDIH · Traditional Bayer Corp.06/26/2000SE
K961656Test-Mate Che Cholinesterase Test SystemDIH · Traditional Eqm Research, Inc.11/26/1996SE
K943367Il Test CholinesteraseDIH · Traditional Instrumentation Laboratory CO02/05/1996SE
K955498Cholinesterase Assay Kit, Catalogue# 300-05DIH · Traditional Diagnostic Chemicals , Ltd.01/24/1996SE

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Questions and answers

When was Olympus Cholinesterase Reagent (Catalog Number OSR6114) cleared by the FDA?

Olympus Cholinesterase Reagent (Catalog Number OSR6114) (K030045) received a 510(k) decision of Substantially Equivalent on February 21, 2003, 46 days after the submission was received.

What is the product code of K030045?

The FDA product code is DIH – Colorimetry, Cholinesterase, a Class I (low risk) device regulated under 21 CFR 862.3240.