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CENTRIFICHEM SYSTEM 500

K810129 Class I Traditional
Decision Date
1981-02-02
Sponsor / Applicant
Union Carbide Corp.

Technical Specification

510(k) Submission ID K810129
Product Code JJE
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2160
Decision Date 1981-02-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CENTRIFICHEM SYSTEM 500 received FDA 510(k) clearance under submission number K810129, 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 1981-02-02.

Classification & Regulation

This clearance is catalogued under FDA product code JJE and 21 CFR 862.2160, within the Clinical Chemistry review panel as a Class I device.