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PORTABLE X-RAY SYSTEM (MODEL:EXARO,XRAY2GO)

K141497 Class II Special
Decision Date
2014-08-26
Sponsor / Applicant
Osstem Implant Co., Ltd.

Technical Specification

510(k) Submission ID K141497
Product Code EHD
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.1800
Decision Date 2014-08-26
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PORTABLE X-RAY SYSTEM (MODEL:EXARO,XRAY2GO) received FDA 510(k) clearance under submission number K141497, sponsored by Osstem Implant Co., Ltd.. The device was reviewed via the Special premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2014-08-26.

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.