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ZEUS SCIENTIFIC, INC., THYROGLOBULIN IGG ELISA TEST SYSTEM

K991179 Class II Traditional
Decision Date
1999-06-17
Sponsor / Applicant
Zeus Scientific, Inc.

Technical Specification

510(k) Submission ID K991179
Product Code DDC
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5870
Decision Date 1999-06-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ZEUS SCIENTIFIC, INC., THYROGLOBULIN IGG ELISA TEST SYSTEM received FDA 510(k) clearance under submission number K991179, 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 1999-06-17.

Classification & Regulation

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