i-STAT G3+ cartridge with the i-STAT 1 System

FDA 510(k) K223857 · Abbott Point of Care, Inc.

Substantially Equivalent

510(k) numberK223857

Submission

Device name
i-STAT G3+ cartridge with the i-STAT 1 System
Applicant
Abbott Point of Care, Inc.
Princton, NJ, US
Received
December 23, 2022
Decision date
September 15, 2023
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
CHL – Electrode Measurement, Blood-Gases (Pco2, Po2) And Blood Ph
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1120
Specialty
Clinical Chemistry

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More from Epocal, Inc.

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K244014i-STAT CG4+ cartridge with the i-STAT 1 SystemCHL · Traditional 05/02/2025SE
K240984i-STAT hs-TnI cartridge with the i-STAT 1 SystemMMI · Traditional 01/03/2025SE
K234143i-STAT TBI Cartridge with the i-STAT Alinity SystemQAT · Traditional 03/27/2024SE
K230300i-STAT CG8+ cartridge with the i-STAT 1 SystemJFP · Traditional 10/27/2023SE
K230285i-STAT CG8+ cartridge with the i-STAT 1 SystemCHL · Traditional 10/27/2023SE
K230275i-STAT CG8+ cartridge with the i-STAT 1 SystemJGS · Traditional 10/27/2023SE
K223755i-STAT G cartridge with the i-STAT 1 SystemCGA · Traditional 09/11/2023SE
K223710i-STAT CG8+ cartridge with the i-STAT 1 SystemCGA · Traditional 07/28/2023SE

Questions and answers

When was i-STAT G3+ cartridge with the i-STAT 1 System cleared by the FDA?

i-STAT G3+ cartridge with the i-STAT 1 System (K223857) received a 510(k) decision of Substantially Equivalent on September 15, 2023, 266 days after the submission was received.

What is the product code of K223857?

The FDA product code is CHL – Electrode Measurement, Blood-Gases (Pco2, Po2) And Blood Ph, a Class II (moderate risk) device regulated under 21 CFR 862.1120.