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QBC HEMACAN HEMATOLOGY SYSTEM

K923121 Class II Traditional
Decision Date
1992-09-22
Sponsor / Applicant
Bd Becton Dickinson Vacutainer Systems Preanalytic

Technical Specification

510(k) Submission ID K923121
Product Code GKL
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.5200
Decision Date 1992-09-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

QBC HEMACAN HEMATOLOGY SYSTEM received FDA 510(k) clearance under submission number K923121, sponsored by Bd Becton Dickinson Vacutainer Systems Preanalytic. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1992-09-22.

Classification & Regulation

This clearance is catalogued under FDA product code GKL and 21 CFR 864.5200, within the Hematology review panel as a Class II device.