meddevicedb.com FDA Device Reference

EVER-BOND V GLASS LONOMER RESTORATIVE

K843072 Class II Traditional
Decision Date
1984-09-07
Sponsor / Applicant
Kerr Corporation (Danbury)

Technical Specification

510(k) Submission ID K843072
Product Code EBF
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3690
Decision Date 1984-09-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EVER-BOND V GLASS LONOMER RESTORATIVE received FDA 510(k) clearance under submission number K843072, sponsored by Kerr Corporation (Danbury). The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1984-09-07.

Classification & Regulation

This clearance is catalogued under FDA product code EBF and 21 CFR 872.3690, within the Dental review panel as a Class II device.