meddevicedb.com FDA Device Reference

GVC-100

K070840 Class II Traditional
Decision Date
2007-05-15
Sponsor / Applicant
GC America, Inc.

Technical Specification

510(k) Submission ID K070840
Product Code EMA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3275
Decision Date 2007-05-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GVC-100 received FDA 510(k) clearance under submission number K070840, sponsored by GC America, 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 2007-05-15.

Classification & Regulation

This clearance is catalogued under FDA product code EMA and 21 CFR 872.3275, within the Dental review panel as a Class II device.