Abx Pentra 400, Calcium CP, Creatinine CP, Phosphorus CP, Amylase CP, Urine Control L/H

FDA 510(k) K070249 · Horiba Abx

Substantially Equivalent

510(k) numberK070249

Submission

Device name
Abx Pentra 400, Calcium CP, Creatinine CP, Phosphorus CP, Amylase CP, Urine Control L/H
Applicant
Horiba Abx
Montpellier, FR
Received
January 26, 2007
Decision date
April 26, 2007
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
CIC – Cresolphthalein Complexone, Calcium
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1145
Specialty
Clinical Chemistry

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K130870Hitachi Clinical Analyzer S Test Reagent Cartridge Calcium (Ca)CIC · Traditional Hitachi Chemical Diagnostics, Inc.05/02/2013SE
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K053401Spotchem II Chemistry Basic 1 and Chemistry Basic 2 TestsCIC · Traditional Arkray, Inc.03/24/2006SE
K050077Spotchem II Calcium, Magnesium, and Blood Urea Nitrogen TestsCIC · Traditional Arkray, Inc.02/15/2005SE
K041009Raichem Calcium (Ocpc) Liquid ReagentCIC · Traditional Hemagen Diagnostics, Inc.06/25/2004SE
K023105Atac Calcium Reagent and Atac CalibratorCIC · Traditional Elan Diagnostics03/13/2003SE
K013652Wiener Lab. Ca-Color Aa, Model 4 X 50 ML Cat.N 1152002CIC · Traditional Wiener Laboratories Saic12/21/2001SE
K000375Randox CalciumCIC · Traditional Randox Laboratories, Ltd.04/05/2000SE
K991111Buffer Chromogen (R1), Product No. CA110-01, Edta Reagen (R2), Product No. CA110-02CIC · Traditional A.P. Total Care, Inc.05/25/1999SE
K971907Calcium ReagentCIC · Traditional Carolina Liquid Chemistries Corp.06/24/1997SE

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Questions and answers

When was Abx Pentra 400, Calcium CP, Creatinine CP, Phosphorus CP, Amylase CP, Urine Control L/H cleared by the FDA?

Abx Pentra 400, Calcium CP, Creatinine CP, Phosphorus CP, Amylase CP, Urine Control L/H (K070249) received a 510(k) decision of Substantially Equivalent on April 26, 2007, 90 days after the submission was received.

What is the product code of K070249?

The FDA product code is CIC – Cresolphthalein Complexone, Calcium, a Class II (moderate risk) device regulated under 21 CFR 862.1145.