Sentinel Cholinesterase Liquid

FDA 510(k) K051444 · Sentinel Ch. Srl

Substantially Equivalent

510(k) numberK051444

Submission

Device name
Sentinel Cholinesterase Liquid
Applicant
Sentinel Ch. Srl
Milano, IT
Received
June 2, 2005
Decision date
June 20, 2005
Decision
Substantially Equivalent (SESE)
Type
Special 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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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
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 Sentinel Cholinesterase Liquid cleared by the FDA?

Sentinel Cholinesterase Liquid (K051444) received a 510(k) decision of Substantially Equivalent on June 20, 2005, 18 days after the submission was received.

What is the product code of K051444?

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