meddevicedb.com FDA Device Reference

Elements

K151150 Class II Traditional
Decision Date
2015-07-28
Sponsor / Applicant
Pac-Dent International, Inc.

Technical Specification

510(k) Submission ID K151150
Product Code ELW
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3660
Decision Date 2015-07-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Elements received FDA 510(k) clearance under submission number K151150, sponsored by Pac-Dent International, 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 2015-07-28.

Classification & Regulation

This clearance is catalogued under FDA product code ELW and 21 CFR 872.3660, within the Dental review panel as a Class II device.