i-STAT Alinity System with i-STAT Sodium test

FDA 510(k) K153357 · Abbott Point of Care, Inc.

Substantially Equivalent

510(k) numberK153357

Submission

Device name
i-STAT Alinity System with i-STAT Sodium test
Applicant
Abbott Point of Care, Inc.
Princton, NJ, US
Received
November 20, 2015
Decision date
July 8, 2016
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JGS – Electrode, Ion Specific, Sodium
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1665
Specialty
Clinical Chemistry

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More from Instrumentation Laboratory CO

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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
K223857i-STAT G3+ cartridge with the i-STAT 1 SystemCHL · Traditional 09/15/2023SE
K223755i-STAT G cartridge with the i-STAT 1 SystemCGA · Traditional 09/11/2023SE

Questions and answers

When was i-STAT Alinity System with i-STAT Sodium test cleared by the FDA?

i-STAT Alinity System with i-STAT Sodium test (K153357) received a 510(k) decision of Substantially Equivalent on July 8, 2016, 231 days after the submission was received.

What is the product code of K153357?

The FDA product code is JGS – Electrode, Ion Specific, Sodium, a Class II (moderate risk) device regulated under 21 CFR 862.1665.