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OPTICLONE CD4FITC/CD8 PE MONOCLONAL ANTIBODIES

K952789 Class II Traditional
Decision Date
1995-08-14
Sponsor / Applicant
Immunotech Corp.

Technical Specification

510(k) Submission ID K952789
Product Code GKZ
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.5220
Decision Date 1995-08-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OPTICLONE CD4FITC/CD8 PE MONOCLONAL ANTIBODIES received FDA 510(k) clearance under submission number K952789, sponsored by Immunotech Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1995-08-14.

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.