meddevicedb.com FDA Device Reference

EzDent-i / E2 / Prora View

K161117 Class II Special
Decision Date
2016-05-13
Sponsor / Applicant
Ewoosoft Co., Ltd.

Technical Specification

510(k) Submission ID K161117
Product Code LLZ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2050
Decision Date 2016-05-13
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EzDent-i / E2 / Prora View received FDA 510(k) clearance under submission number K161117, sponsored by Ewoosoft Co., Ltd.. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2016-05-13.

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.