Synchron Systems Cholinesterase (Chex) Model A53722

FDA 510(k) K103373 · Beckman Coulter, Inc.

Substantially Equivalent

510(k) numberK103373

Submission

Device name
Synchron Systems Cholinesterase (Chex) Model A53722
Applicant
Beckman Coulter, Inc.
Brea, CA, US
Received
November 17, 2010
Decision date
February 7, 2011
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary 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

Other 510(k)s with product code DIH

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K061093Cholinesterase GEN.2 Test SystemDIH · Traditional Roche Diagnostics Corp.07/03/2006SE
K051444Sentinel Cholinesterase LiquidDIH · Special Sentinel Ch. Srl06/20/2005SE
K030045Olympus Cholinesterase Reagent (Catalog Number OSR6114)DIH · Traditional Olympus America, Inc.02/21/2003SE
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 Synchron Systems Cholinesterase (Chex) Model A53722 cleared by the FDA?

Synchron Systems Cholinesterase (Chex) Model A53722 (K103373) received a 510(k) decision of Substantially Equivalent on February 7, 2011, 82 days after the submission was received.

What is the product code of K103373?

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