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TOTAL T3-RIA KIT COATED TUBE RADIOIMMUNOASSAY KIT

K870968 Class II Traditional
Decision Date
1987-06-22
Sponsor / Applicant
Canadian Bioclinical, Ltd.

Technical Specification

510(k) Submission ID K870968
Product Code CDP
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1710
Decision Date 1987-06-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TOTAL T3-RIA KIT COATED TUBE RADIOIMMUNOASSAY KIT received FDA 510(k) clearance under submission number K870968, sponsored by Canadian Bioclinical, Ltd.. 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 1987-06-22.

Classification & Regulation

This clearance is catalogued under FDA product code CDP and 21 CFR 862.1710, within the Clinical Chemistry review panel as a Class II device.