meddevicedb.com FDA Device Reference

FLUOREVER(R) LIGHT CURE CERAMIC VENEER CEMENT

K890608 Class II Traditional
Decision Date
1989-04-17
Sponsor / Applicant
Macrochem Corp.

Technical Specification

510(k) Submission ID K890608
Product Code EMA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3275
Decision Date 1989-04-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FLUOREVER(R) LIGHT CURE CERAMIC VENEER CEMENT received FDA 510(k) clearance under submission number K890608, sponsored by Macrochem Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1989-04-17.

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.