meddevicedb.com FDA Device Reference

ALPHA-CORE DC

K070191 Class II Traditional
Decision Date
2007-03-07
Sponsor / Applicant
Dental Technologies, Inc.

Technical Specification

510(k) Submission ID K070191
Product Code EBF
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3690
Decision Date 2007-03-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ALPHA-CORE DC received FDA 510(k) clearance under submission number K070191, sponsored by Dental Technologies, 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 2007-03-07.

Classification & Regulation

This clearance is catalogued under FDA product code EBF and 21 CFR 872.3690, within the Dental review panel as a Class II device.