Sodium and Potassium Standard

FDA 510(k) K895717 · Data Medical Associates, Inc.

Substantially Equivalent

510(k) numberK895717

Submission

Device name
Sodium and Potassium Standard
Applicant
Data Medical Associates, Inc.
Arlington, TX, US
Received
September 25, 1989
Decision date
January 11, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JIX – Calibrator, Multi-Analyte Mixture
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1150
Specialty
Clinical Chemistry

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Questions and answers

When was Sodium and Potassium Standard cleared by the FDA?

Sodium and Potassium Standard (K895717) received a 510(k) decision of Substantially Equivalent on January 11, 1990, 108 days after the submission was received.

What is the product code of K895717?

The FDA product code is JIX – Calibrator, Multi-Analyte Mixture, a Class II (moderate risk) device regulated under 21 CFR 862.1150.