Model 654 a Sodium, Potassium & Lithium Ise Analy

FDA 510(k) K884769 · Ciba Corning Diagnostics Corp.

Substantially Equivalent

510(k) numberK884769

Submission

Device name
Model 654 a Sodium, Potassium & Lithium Ise Analy
Applicant
Ciba Corning Diagnostics Corp.
East Walpole, MA, US
Received
November 14, 1988
Decision date
January 17, 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 Model 654 a Sodium, Potassium & Lithium Ise Analy cleared by the FDA?

Model 654 a Sodium, Potassium & Lithium Ise Analy (K884769) received a 510(k) decision of Substantially Equivalent on January 17, 1989, 64 days after the submission was received.

What is the product code of K884769?

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