meddevicedb.com FDA Device Reference

RADIOIMMUNOASSAY, TOTAL TRIIODOTHRONIE

K810351 Class II Traditional
Decision Date
1981-02-23
Sponsor / Applicant
Endocrine-Metabolic Center

Technical Specification

510(k) Submission ID K810351
Product Code CDP
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1710
Decision Date 1981-02-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RADIOIMMUNOASSAY, TOTAL TRIIODOTHRONIE received FDA 510(k) clearance under submission number K810351, sponsored by Endocrine-Metabolic Center. 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 1981-02-23.

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.