Calcium2

FDA 510(k) K244042 · Abbott Ireland

Substantially Equivalent

510(k) numberK244042

Submission

Device name
Calcium2
Applicant
Abbott Ireland
Lisnamuck, IE
Received
December 30, 2024
Decision date
February 10, 2025
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
CJY – Azo Dye, Calcium
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1145
Specialty
Clinical Chemistry

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K191396Yumizen C1200 Calcium AS, Yumizen C1200 Creatinine JaffeCJY · Traditional Horiba Abx SAS07/26/2019SE
K182042Randox Calcium (Ca)CJY · Traditional Randox Laboratories, Ltd.10/23/2018SE
K151113ELITech Clinical Systems CALCIUM ARSENAZOCJY · Traditional Elitechgroup07/22/2015SE
K123171Abx Pentra Calcium AS CP, Abx Pentra Urine Control L/H, Abx Pentra Multical, Abx Pentra…CJY · Abbreviated Horiba Abx SAS07/03/2013SE
K120626Eon Calcium RegentCJY · Traditional Vital Diagnostics (Manufacturing) Ptyltd08/22/2012SE
K083386Advia Chemistry CALCIUM_2 (CA_2) Method, Models P/M 02189699 (40 ML Fill), P/N 02189915…CJY · Traditional Siemens Healthcare Diagnostics04/02/2009SE
K072356S-Test CaCJY · Traditional Alfa Wassermann Diagnostic Technologies, Inc.06/24/2008SE
K073355Calcium, Scal, Nortrol, AbtrolCJY · Traditional Thermofisher Scientific OY02/28/2008SE
K072443Vitros Chemistry Products Ca DT Slides and DT Calibrator Kit and Vitros Ca AssayCJY · Special Ortho-Clinical Diagnostics, Inc.09/24/2007SE
K072440Vitros Chemistry Products: Ca Slides (Model: 145 0261), Calibrators Kit 1 (Model: 188…CJY · Special Ortho-Clinical Diagnostics, Inc.09/20/2007SE

More from Ortho-Clinical Diagnostics, Inc.

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Questions and answers

When was Calcium2 cleared by the FDA?

Calcium2 (K244042) received a 510(k) decision of Substantially Equivalent on February 10, 2025, 42 days after the submission was received.

What is the product code of K244042?

The FDA product code is CJY – Azo Dye, Calcium, a Class II (moderate risk) device regulated under 21 CFR 862.1145.