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MODIFICATION TO ZEUS SCIENTIFIC, INC., TPO IGG ELISA TEST SYSTEM

K000362 Class II Special
Decision Date
2000-02-18
Sponsor / Applicant
Zeus Scientific, Inc.

Technical Specification

510(k) Submission ID K000362
Product Code JZO
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5870
Decision Date 2000-02-18
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODIFICATION TO ZEUS SCIENTIFIC, INC., TPO IGG ELISA TEST SYSTEM received FDA 510(k) clearance under submission number K000362, sponsored by Zeus Scientific, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 2000-02-18.

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.