SelectaLyte Electrolyte Analyzer (Na+, K+, Cl-)

FDA 510(k) K171476 · Awareness Technology, Inc.

Substantially Equivalent

510(k) numberK171476

Submission

Device name
SelectaLyte Electrolyte Analyzer (Na+, K+, Cl-)
Applicant
Awareness Technology, Inc.
Palm City, FL, US
Received
May 19, 2017
Decision date
February 27, 2018
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

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

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Questions and answers

When was SelectaLyte Electrolyte Analyzer (Na+, K+, Cl-) cleared by the FDA?

SelectaLyte Electrolyte Analyzer (Na+, K+, Cl-) (K171476) received a 510(k) decision of Substantially Equivalent on February 27, 2018, 284 days after the submission was received.

What is the product code of K171476?

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