meddevicedb.com FDA Device Reference

A-DEC 200 DENTAL SYSTEM

K102234 Class I Traditional
Decision Date
2010-11-24
Sponsor / Applicant
A-Dec, Inc.

Technical Specification

510(k) Submission ID K102234
Product Code EIA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6640
Decision Date 2010-11-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

A-DEC 200 DENTAL SYSTEM received FDA 510(k) clearance under submission number K102234, sponsored by A-Dec, 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 2010-11-24.

Classification & Regulation

This clearance is catalogued under FDA product code EIA and 21 CFR 872.6640, within the Dental review panel as a Class I device.