meddevicedb.com FDA Device Reference

SIMULTEST IMK FOR FACS ANALYZER OR FACSCAN

K890349 Class II Traditional
Decision Date
1989-12-29
Sponsor / Applicant
Becton Dickinson Immunocytometry Systems

Technical Specification

510(k) Submission ID K890349
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

SIMULTEST IMK FOR FACS ANALYZER OR FACSCAN received FDA 510(k) clearance under submission number K890349, 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 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.