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IFA HEP2 KIT FOR THE DETECTION OF ANTINUCLEAR ANTIBODIES

K970198 Class II Traditional
Decision Date
1997-02-20
Sponsor / Applicant
Scimedx Corp.

Technical Specification

510(k) Submission ID K970198
Product Code DHN
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5100
Decision Date 1997-02-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IFA HEP2 KIT FOR THE DETECTION OF ANTINUCLEAR ANTIBODIES received FDA 510(k) clearance under submission number K970198, sponsored by Scimedx Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 1997-02-20.

Classification & Regulation

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