meddevicedb.com FDA Device Reference

X-SMART EASY

K092614 Class I Traditional
Decision Date
2009-12-02
Sponsor / Applicant
Dentsply Interntional

Technical Specification

510(k) Submission ID K092614
Product Code EKX
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4200
Decision Date 2009-12-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

X-SMART EASY received FDA 510(k) clearance under submission number K092614, sponsored by Dentsply Interntional. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2009-12-02.

Classification & Regulation

This clearance is catalogued under FDA product code EKX and 21 CFR 872.4200, within the Dental review panel as a Class I device.