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VISIQUANT ANTI-NUCLEAR ANTIBODY TEST SYSTEM

K022800 Class II Traditional
Decision Date
2002-11-25
Sponsor / Applicant
Hyperion, Inc.

Technical Specification

510(k) Submission ID K022800
Product Code DHN
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5100
Decision Date 2002-11-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VISIQUANT ANTI-NUCLEAR ANTIBODY TEST SYSTEM received FDA 510(k) clearance under submission number K022800, sponsored by Hyperion, 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 2002-11-25.

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.