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TRI TEST REAGENT CD4 FIT C/CD8 PE/CD3 PERCP WITH TRUCOUNT ABSOLUTE COUNT TUBES

K971205 Class II Traditional
Decision Date
1997-12-01
Sponsor / Applicant
Becton Dickinson Immunocytometry Systems

Technical Specification

510(k) Submission ID K971205
Product Code GKZ
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.5220
Decision Date 1997-12-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TRI TEST REAGENT CD4 FIT C/CD8 PE/CD3 PERCP WITH TRUCOUNT ABSOLUTE COUNT TUBES received FDA 510(k) clearance under submission number K971205, sponsored by Becton Dickinson Immunocytometry Systems. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1997-12-01.

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.