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CELL-DYN 1500 MULTI-PARAMETER HEMATOLOGY ANALYZER

K854368 Class II Traditional
Decision Date
1986-01-01
Sponsor / Applicant
Abbott Diagnostics

Technical Specification

510(k) Submission ID K854368
Product Code GKZ
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.5220
Decision Date 1986-01-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CELL-DYN 1500 MULTI-PARAMETER HEMATOLOGY ANALYZER received FDA 510(k) clearance under submission number K854368, sponsored by Abbott Diagnostics. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1986-01-01.

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.