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

K171476 Class II Traditional
Decision Date
2018-02-27
Sponsor / Applicant
Awareness Technology, Inc.

Technical Specification

510(k) Submission ID K171476
Product Code JGS
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1665
Decision Date 2018-02-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SelectaLyte Electrolyte Analyzer (Na+, K+, Cl-) received FDA 510(k) clearance under submission number K171476, sponsored by Awareness Technology, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 2018-02-27.

Classification & Regulation

This clearance is catalogued under FDA product code JGS and 21 CFR 862.1665, within the Clinical Chemistry review panel as a Class II device.