meddevicedb.com FDA Device Reference

RADIAS FERRITIN ENZYME IMMUNOASSAY

K933314 Class II Traditional
Decision Date
1993-09-08
Sponsor / Applicant
Bio-Rad

Technical Specification

510(k) Submission ID K933314
Product Code DEW
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5510
Decision Date 1993-09-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RADIAS FERRITIN ENZYME IMMUNOASSAY received FDA 510(k) clearance under submission number K933314, 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 1993-09-08.

Classification & Regulation

This clearance is catalogued under FDA product code DEW and 21 CFR 866.5510, within the Immunology review panel as a Class II device.