meddevicedb.com FDA Device Reference

ADC DENTAL

K021542 Class II Traditional
Decision Date
2002-08-06
Sponsor / Applicant
Agfa Corp.

Technical Specification

510(k) Submission ID K021542
Product Code MUH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.1800
Decision Date 2002-08-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ADC DENTAL received FDA 510(k) clearance under submission number K021542, sponsored by Agfa Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2002-08-06.

Classification & Regulation

This clearance is catalogued under FDA product code MUH and 21 CFR 872.1800, within the Dental review panel as a Class II device.