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TOTAL CO2

K951221 Class II Traditional
Decision Date
1996-02-15
Sponsor / Applicant
Randox Laboratories, Ltd.

Technical Specification

510(k) Submission ID K951221
Product Code KHS
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1160
Decision Date 1996-02-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TOTAL CO2 received FDA 510(k) clearance under submission number K951221, sponsored by Randox Laboratories, Ltd.. 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 1996-02-15.

Classification & Regulation

This clearance is catalogued under FDA product code KHS and 21 CFR 862.1160, within the Clinical Chemistry review panel as a Class II device.