Potassium and Sodium Electrolyte Analyzer

FDA 510(k) K890792 · Ionetics, Inc.

Substantially Equivalent

510(k) numberK890792

Submission

Device name
Potassium and Sodium Electrolyte Analyzer
Applicant
Ionetics, Inc.
Costa Mesa, CA, US
Received
February 17, 1989
Decision date
May 3, 1989
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CEM – Electrode, Ion Specific, Potassium
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1600
Specialty
Clinical Chemistry

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More from Beckman Coulter, Inc.

510(k)DeviceDecision
K932179Model 400/450 Electrolyte AnalyzerJGS · Traditional 11/17/1993SE
K895397Calcium and PH Electrolyte AnalyzerJFP · Traditional 12/12/1989SE
K863907Modified Sodium ElectrodeJGS · Traditional 12/10/1986SE
K851808Electrolyte AnalyzerCEM · Traditional 06/25/1985SE
K830130Miniature Ion Selective ElectrodesJSG · Traditional 03/07/1983SE
K802856Miniature Ion Selective ElectrodesJFP · Traditional 01/28/1981SE

Questions and answers

When was Potassium and Sodium Electrolyte Analyzer cleared by the FDA?

Potassium and Sodium Electrolyte Analyzer (K890792) received a 510(k) decision of Substantially Equivalent on May 3, 1989, 75 days after the submission was received.

What is the product code of K890792?

The FDA product code is CEM – Electrode, Ion Specific, Potassium, a Class II (moderate risk) device regulated under 21 CFR 862.1600.