meddevicedb.com FDA Device Reference

FINESSE LOW-FUSING PORCELAIN SYSTEM

K954761 Class II Traditional
Decision Date
1995-11-02
Sponsor / Applicant
Dentsply Intl.

Technical Specification

510(k) Submission ID K954761
Product Code EIH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6660
Decision Date 1995-11-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FINESSE LOW-FUSING PORCELAIN SYSTEM received FDA 510(k) clearance under submission number K954761, sponsored by Dentsply Intl.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1995-11-02.

Classification & Regulation

This clearance is catalogued under FDA product code EIH and 21 CFR 872.6660, within the Dental review panel as a Class II device.