meddevicedb.com FDA Device Reference

GC FUJI LINING LC PASTE PAK

K020117 Class II Traditional
Decision Date
2002-02-28
Sponsor / Applicant
GC America, Inc.

Technical Specification

510(k) Submission ID K020117
Product Code EMA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3275
Decision Date 2002-02-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GC FUJI LINING LC PASTE PAK received FDA 510(k) clearance under submission number K020117, 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 2002-02-28.

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.