Technicon Dax System - Potassium (Ise) Method

FDA 510(k) K895664 · Technicon Instruments Corp.

Substantially Equivalent

510(k) numberK895664

Submission

Device name
Technicon Dax System - Potassium (Ise) Method
Applicant
Technicon Instruments Corp.
Tarrytown, NY, US
Received
September 20, 1989
Decision date
November 14, 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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Questions and answers

When was Technicon Dax System - Potassium (Ise) Method cleared by the FDA?

Technicon Dax System - Potassium (Ise) Method (K895664) received a 510(k) decision of Substantially Equivalent on November 14, 1989, 55 days after the submission was received.

What is the product code of K895664?

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