meddevicedb.com FDA Device Reference

NEW OUTLINE

K023079 Class II Traditional
Decision Date
2002-10-30
Sponsor / Applicant
Anaxdent GmbH

Technical Specification

510(k) Submission ID K023079
Product Code EBG
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3770
Decision Date 2002-10-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NEW OUTLINE received FDA 510(k) clearance under submission number K023079, sponsored by Anaxdent GmbH. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2002-10-30.

Classification & Regulation

This clearance is catalogued under FDA product code EBG and 21 CFR 872.3770, within the Dental review panel as a Class II device.