meddevicedb.com FDA Device Reference

Portable X-ray System

K172928 Class II Traditional
Decision Date
2018-03-16
Sponsor / Applicant
Rolence Enterprise, Inc.

Technical Specification

510(k) Submission ID K172928
Product Code EHD
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.1800
Decision Date 2018-03-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Portable X-ray System received FDA 510(k) clearance under submission number K172928, sponsored by Rolence Enterprise, 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 2018-03-16.

Classification & Regulation

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