meddevicedb.com FDA Device Reference

RENAISSANCE

K844395 Class II Traditional
Decision Date
1985-01-09
Sponsor / Applicant
Williams Gold Refining Co., Inc.

Technical Specification

510(k) Submission ID K844395
Product Code EJT
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3060
Decision Date 1985-01-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RENAISSANCE received FDA 510(k) clearance under submission number K844395, sponsored by Williams Gold Refining Co., Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1985-01-09.

Classification & Regulation

This clearance is catalogued under FDA product code EJT and 21 CFR 872.3060, within the Dental review panel as a Class II device.