Piccolo Chloride Test System

FDA 510(k) K010670 · Abaxis, Inc.

Substantially Equivalent

510(k) numberK010670

Submission

Device name
Piccolo Chloride Test System
Applicant
Abaxis, Inc.
Union City, CA, US
Received
March 6, 2001
Decision date
April 26, 2001
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
CHJ – Mercuric Thiocyanate, Colorimetry, Chloride
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1170
Specialty
Clinical Chemistry

Other 510(k)s with product code CHJ

510(k)DeviceApplicantDecision
K945408340-CHLORIDE for Discrete Random Access AnalyzerCHJ · Traditional Catachem, Inc.02/22/1995SE
K943006Chloride QvetCHJ · Traditional Prisma Systems12/07/1994SE
K934136Olympus Chloride Reagent, ModificationCHJ · Traditional Olympus Corp.11/05/1993SE
K932528Olympus Chlorid Reagent, ModifiedCHJ · Traditional Olympus Corp.09/17/1993SE
K925338Olympus Chloride ReagentCHJ · Traditional Olympus Corp.12/11/1992SE
K922921King Diagnostics Chloride ReagentCHJ · Traditional King Diagnostics, Inc.10/05/1992SE
K923610Olympus Chloride ReagentCHJ · Traditional Olympus Corp.10/02/1992SE
K923036Urine ChlorideCHJ · Traditional Heraeus Kulzer, Inc.09/09/1992SE
K911297Chloride ReagentCHJ · Traditional Intersect Systems, Inc.04/16/1991SE
K910133Chloride Reagent (C1), Catalog No. DR0011/MODIFIEDCHJ · Traditional Olympus Corp.02/27/1991SE

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K091052Piccolo C-Reactive Protein (CRP) Test SystemDCN · Traditional 01/15/2010SE
K091910Piccolo Magnesium Test SystemJGJ · Special 10/01/2009SE
K051108Piccolo Lactate Dephydrogenase Test SystemCFJ · Traditional 07/08/2005SE
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Questions and answers

When was Piccolo Chloride Test System cleared by the FDA?

Piccolo Chloride Test System (K010670) received a 510(k) decision of Substantially Equivalent on April 26, 2001, 51 days after the submission was received.

What is the product code of K010670?

The FDA product code is CHJ – Mercuric Thiocyanate, Colorimetry, Chloride, a Class II (moderate risk) device regulated under 21 CFR 862.1170.