meddevicedb.com FDA Device Reference

COULTER CLONE T4 MONOCLONAL ANTIBODY

K893852 Class II Traditional
Decision Date
1990-03-02
Sponsor / Applicant
Coulter Immunology

Technical Specification

510(k) Submission ID K893852
Product Code GKZ
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.5220
Decision Date 1990-03-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

COULTER CLONE T4 MONOCLONAL ANTIBODY received FDA 510(k) clearance under submission number K893852, sponsored by Coulter Immunology. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1990-03-02.

Classification & Regulation

This clearance is catalogued under FDA product code GKZ and 21 CFR 864.5220, within the Hematology review panel as a Class II device.