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LIQUICHEK ANA CONTROL, EIA SCREEN, MODEL 205

K984473 Class II Traditional
Decision Date
1998-12-22
Sponsor / Applicant
Bio-Rad

Technical Specification

510(k) Submission ID K984473
Product Code LKJ
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5100
Decision Date 1998-12-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LIQUICHEK ANA CONTROL, EIA SCREEN, MODEL 205 received FDA 510(k) clearance under submission number K984473, sponsored by Bio-Rad. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 1998-12-22.

Classification & Regulation

This clearance is catalogued under FDA product code LKJ and 21 CFR 866.5100, within the Immunology review panel as a Class II device.