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HEP-2 ANA TEST SYSTEM WITH IF-AIM TECHNOLOGY

K001556 Class II Traditional
Decision Date
2000-08-21
Sponsor / Applicant
The Binding Site, Ltd.

Technical Specification

510(k) Submission ID K001556
Product Code DHN
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5100
Decision Date 2000-08-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEP-2 ANA TEST SYSTEM WITH IF-AIM TECHNOLOGY received FDA 510(k) clearance under submission number K001556, sponsored by The Binding Site, Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 2000-08-21.

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.