meddevicedb.com FDA Device Reference

DENTAL MERCURY

K093587 Class II Traditional
Decision Date
2010-01-21
Sponsor / Applicant
Dmg USA, Inc.

Technical Specification

510(k) Submission ID K093587
Product Code ELY
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3070
Decision Date 2010-01-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DENTAL MERCURY received FDA 510(k) clearance under submission number K093587, sponsored by Dmg USA, 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 2010-01-21.

Classification & Regulation

This clearance is catalogued under FDA product code ELY and 21 CFR 872.3070, within the Dental review panel as a Class II device.