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ENZYME-LINKED FLUORESCENT IMMUNOASSAY

K943811 Class I Traditional
Decision Date
1994-11-02
Sponsor / Applicant
Biomerieux Vitek, Inc.

Technical Specification

510(k) Submission ID K943811
Product Code CFT
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1625
Decision Date 1994-11-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ENZYME-LINKED FLUORESCENT IMMUNOASSAY received FDA 510(k) clearance under submission number K943811, sponsored by Biomerieux Vitek, 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 1994-11-02.

Classification & Regulation

This clearance is catalogued under FDA product code CFT and 21 CFR 862.1625, within the Clinical Chemistry review panel as a Class I device.