meddevicedb.com FDA Device Reference

3M RELY X VENEER CEMENT TRY-IN PASTER

K002452 Class II Traditional
Decision Date
2000-09-28
Sponsor / Applicant
3M Company

Technical Specification

510(k) Submission ID K002452
Product Code EMA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3275
Decision Date 2000-09-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

3M RELY X VENEER CEMENT TRY-IN PASTER received FDA 510(k) clearance under submission number K002452, sponsored by 3M Company. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2000-09-28.

Classification & Regulation

This clearance is catalogued under FDA product code EMA and 21 CFR 872.3275, within the Dental review panel as a Class II device.