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HEMOCHRON VERIGY SYSTEM/FACTOR VI QUALIFY SYSTEM

K940957 Class II Traditional
Decision Date
1994-10-18
Sponsor / Applicant
International Technidyne Corp.

Technical Specification

510(k) Submission ID K940957
Product Code JPA
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.5425
Decision Date 1994-10-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEMOCHRON VERIGY SYSTEM/FACTOR VI QUALIFY SYSTEM received FDA 510(k) clearance under submission number K940957, sponsored by International Technidyne 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 1994-10-18.

Classification & Regulation

This clearance is catalogued under FDA product code JPA and 21 CFR 864.5425, within the Hematology review panel as a Class II device.