meddevicedb.com FDA Device Reference

HUMAN IGG SUBCLASS KIT FOR USE ON THE BECKMAN IMMAGE ANALYSER

K022083 Class II Traditional
Decision Date
2002-07-16
Sponsor / Applicant
The Binding Site, Ltd.

Technical Specification

510(k) Submission ID K022083
Product Code CFN
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5510
Decision Date 2002-07-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HUMAN IGG SUBCLASS KIT FOR USE ON THE BECKMAN IMMAGE ANALYSER received FDA 510(k) clearance under submission number K022083, 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 2002-07-16.

Classification & Regulation

This clearance is catalogued under FDA product code CFN and 21 CFR 866.5510, within the Immunology review panel as a Class II device.