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AUTOMATED BLOOD CELL SEPAR. DISP. SFTWR

K820396 Class II Traditional
Decision Date
1982-04-27
Sponsor / Applicant
Pheragen Technology Corp.

Technical Specification

510(k) Submission ID K820396
Product Code GKT
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.9245
Decision Date 1982-04-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AUTOMATED BLOOD CELL SEPAR. DISP. SFTWR received FDA 510(k) clearance under submission number K820396, sponsored by Pheragen Technology Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1982-04-27.

Classification & Regulation

This clearance is catalogued under FDA product code GKT and 21 CFR 864.9245, within the Hematology review panel as a Class II device.