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BECKMAN ELECTROLYTE-2 SODIUM/POTASSIUM

K801896 Class II Traditional
Decision Date
1980-09-16
Sponsor / Applicant
Beckman Instruments, Inc.

Technical Specification

510(k) Submission ID K801896
Product Code JGS
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1665
Decision Date 1980-09-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BECKMAN ELECTROLYTE-2 SODIUM/POTASSIUM received FDA 510(k) clearance under submission number K801896, sponsored by Beckman Instruments, 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 1980-09-16.

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.