meddevicedb.com FDA Device Reference

CERCON BASE

K013230 Class II Traditional
Decision Date
2001-10-25
Sponsor / Applicant
Degussa - Ney Dental, Inc.

Technical Specification

510(k) Submission ID K013230
Product Code EIH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6660
Decision Date 2001-10-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CERCON BASE received FDA 510(k) clearance under submission number K013230, sponsored by Degussa - Ney Dental, 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 2001-10-25.

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.