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CYTO-STAT/COULTER CLONE T4-RD1/T8-FITC MONO ANTI

K895917 Class II Traditional
Decision Date
1989-12-29
Sponsor / Applicant
Coulter Immunology

Technical Specification

510(k) Submission ID K895917
Product Code GKZ
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.5220
Decision Date 1989-12-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CYTO-STAT/COULTER CLONE T4-RD1/T8-FITC MONO ANTI received FDA 510(k) clearance under submission number K895917, 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 1989-12-29.

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.