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QBC STAR CENTRIFUGAL HEMATOLOGY SYSTEM

K992849 Class II Special
Decision Date
1999-09-23
Sponsor / Applicant
Bd Becton Dickinson Vacutainer Systems Preanalytic

Technical Specification

510(k) Submission ID K992849
Product Code GKZ
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.5220
Decision Date 1999-09-23
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

QBC STAR CENTRIFUGAL HEMATOLOGY SYSTEM received FDA 510(k) clearance under submission number K992849, sponsored by Bd Becton Dickinson Vacutainer Systems Preanalytic. The device was reviewed via the Special premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1999-09-23.

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.