meddevicedb.com FDA Device Reference

X-IMAGE DIGITAL X-RAY SYSTEM

K020588 Class II Traditional
Decision Date
2002-06-13
Sponsor / Applicant
Escape Technology, Inc.

Technical Specification

510(k) Submission ID K020588
Product Code MUH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.1800
Decision Date 2002-06-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

X-IMAGE DIGITAL X-RAY SYSTEM received FDA 510(k) clearance under submission number K020588, sponsored by Escape Technology, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2002-06-13.

Classification & Regulation

This clearance is catalogued under FDA product code MUH and 21 CFR 872.1800, within the Dental review panel as a Class II device.