meddevicedb.com FDA Device Reference

DENTAL-QUECKSILBER (DENTAL MERCURY)

K902388 Class II Traditional
Decision Date
1990-06-28
Sponsor / Applicant
Degussa AG

Technical Specification

510(k) Submission ID K902388
Product Code ELY
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3070
Decision Date 1990-06-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DENTAL-QUECKSILBER (DENTAL MERCURY) received FDA 510(k) clearance under submission number K902388, sponsored by Degussa AG. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1990-06-28.

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.