meddevicedb.com FDA Device Reference

CENTRIA SYSTEM

K790550 Class I Traditional
Decision Date
1979-05-07
Sponsor / Applicant
Union Carbide Corp.

Technical Specification

510(k) Submission ID K790550
Product Code JJG
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2140
Decision Date 1979-05-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CENTRIA SYSTEM received FDA 510(k) clearance under submission number K790550, sponsored by Union Carbide Corp.. 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 1979-05-07.

Classification & Regulation

This clearance is catalogued under FDA product code JJG and 21 CFR 862.2140, within the Clinical Chemistry review panel as a Class I device.