meddevicedb.com FDA Device Reference

TEST, (IVDP) THYROID ANTIBODY

K760154 Class II Traditional
Decision Date
1976-07-20
Sponsor / Applicant
Zeus Scientific, Inc.

Technical Specification

510(k) Submission ID K760154
Product Code JZO
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5870
Decision Date 1976-07-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TEST, (IVDP) THYROID ANTIBODY received FDA 510(k) clearance under submission number K760154, sponsored by Zeus Scientific, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 1976-07-20.

Classification & Regulation

This clearance is catalogued under FDA product code JZO and 21 CFR 866.5870, within the Immunology review panel as a Class II device.