meddevicedb.com FDA Device Reference

ZENIS, PICTURE ARCHIVING AND COMMUNICATIONS SYSTEM

K103181 Class II Traditional
Decision Date
2011-08-26
Sponsor / Applicant
Genoray Co., Ltd.

Technical Specification

510(k) Submission ID K103181
Product Code LLZ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2050
Decision Date 2011-08-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ZENIS, PICTURE ARCHIVING AND COMMUNICATIONS SYSTEM received FDA 510(k) clearance under submission number K103181, sponsored by Genoray Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2011-08-26.

Classification & Regulation

This clearance is catalogued under FDA product code LLZ and 21 CFR 892.2050, within the Radiology review panel as a Class II device.