Ion Selective Electrode Subsystem of Para. Analyt.

FDA 510(k) K882104 · Paramax Systems Div. Baxter Healthcare

Substantially Equivalent

510(k) numberK882104

Submission

Device name
Ion Selective Electrode Subsystem of Para. Analyt.
Applicant
Paramax Systems Div. Baxter Healthcare
Santa Ana, CA, US
Received
May 19, 1988
Decision date
July 5, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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

Other 510(k)s with product code JGS

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K222438A-LYTE® Integrated Multisensor (IMT Na K Cl)JGS · Traditional Siemens Healthcare Diagnostics, Inc.07/25/2023SE
K220977ISE Reagents, Glucose, CRP Latex, DxC 500 AU Clinical Chemistry AnalyzerJGS · Traditional Beckman Coulter Laboratory Systems (Suzhou) Co.…07/20/2023SE
K213486GLP systems TrackJGS · Traditional Abbott Laboratories03/10/2022SE
K200403Stat Profile Prime Plus Analyzer SystemJGS · Traditional Nova Biomedical Corporation04/14/2020SE
K183688i-STAT CHEM8+ cartridge with the i-STAT 1 SystemJGS · Traditional Abbott Point of Care, Inc.02/07/2020SE
K191365Stat Profile Prime ES Comp Plus Analyzer SystemJGS · Traditional Nova Biomedical Corporation07/19/2019SE
K172232LIASYS 600 Electrolyte Measurement System, LIASYS 600 Creatinine reagent, LIASYS 600JGS · Traditional Ams Diagnostics06/12/2019SE
K183549GEM Premier ChemSTATJGS · Traditional Instrumentation Laboratory CO02/16/2019SE

Questions and answers

When was Ion Selective Electrode Subsystem of Para. Analyt. cleared by the FDA?

Ion Selective Electrode Subsystem of Para. Analyt. (K882104) received a 510(k) decision of Substantially Equivalent on July 5, 1988, 47 days after the submission was received.

What is the product code of K882104?

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