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UNIWEB, VERSION 5.0

K071166 Class II Abbreviated
Decision Date
2007-07-23
Sponsor / Applicant
Electronic Business Machine Co., Ltd. (Ebm)

Technical Specification

510(k) Submission ID K071166
Product Code LLZ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2050
Decision Date 2007-07-23
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

UNIWEB, VERSION 5.0 received FDA 510(k) clearance under submission number K071166, sponsored by Electronic Business Machine Co., Ltd. (Ebm). The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2007-07-23.

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.