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ANTI-LEU-4 FITC LYSIN C BUFFER

K842218 Class II Traditional
Decision Date
1984-12-27
Sponsor / Applicant
Bd Becton Dickinson Vacutainer Systems Preanalytic

Technical Specification

510(k) Submission ID K842218
Product Code LIZ
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.5220
Decision Date 1984-12-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ANTI-LEU-4 FITC LYSIN C BUFFER received FDA 510(k) clearance under submission number K842218, 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 1984-12-27.

Classification & Regulation

This clearance is catalogued under FDA product code LIZ and 21 CFR 864.5220, within the Hematology review panel as a Class II device.