meddevicedb.com FDA Device Reference

EXTRACTABLE NUCLEAR ANTIGEN ASSAY

K840221 Class II Traditional
Decision Date
1984-05-22
Sponsor / Applicant
Zeus Scientific, Inc.

Technical Specification

510(k) Submission ID K840221
Product Code LLL
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5100
Decision Date 1984-05-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EXTRACTABLE NUCLEAR ANTIGEN ASSAY received FDA 510(k) clearance under submission number K840221, 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 1984-05-22.

Classification & Regulation

This clearance is catalogued under FDA product code LLL and 21 CFR 866.5100, within the Immunology review panel as a Class II device.