meddevicedb.com FDA Device Reference

RADIAS TSH ENZYME IMMUNOASSAY

K931061 Class II Traditional
Decision Date
1993-06-16
Sponsor / Applicant
Bio-Rad

Technical Specification

510(k) Submission ID K931061
Product Code JLW
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1690
Decision Date 1993-06-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RADIAS TSH ENZYME IMMUNOASSAY received FDA 510(k) clearance under submission number K931061, sponsored by Bio-Rad. 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 1993-06-16.

Classification & Regulation

This clearance is catalogued under FDA product code JLW and 21 CFR 862.1690, within the Clinical Chemistry review panel as a Class II device.