meddevicedb.com FDA Device Reference

TEMPO CUSHION TREATMENT DENTURE RELINE ACRYLIC RESIN LIQUID, PROFESSIONAL SIZE PACKAGE AND POWDER

K081514 Class II Traditional
Decision Date
2008-09-22
Sponsor / Applicant
Lang Dental Mfg. Co., Inc.

Technical Specification

510(k) Submission ID K081514
Product Code EBI
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3760
Decision Date 2008-09-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TEMPO CUSHION TREATMENT DENTURE RELINE ACRYLIC RESIN LIQUID, PROFESSIONAL SIZE PACKAGE AND POWDER received FDA 510(k) clearance under submission number K081514, sponsored by Lang Dental Mfg. Co., 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 2008-09-22.

Classification & Regulation

This clearance is catalogued under FDA product code EBI and 21 CFR 872.3760, within the Dental review panel as a Class II device.