meddevicedb.com FDA Device Reference

CUSHIONS, DENTURE ADHESIVE, ALL-DAY

K770413 Class II Traditional
Decision Date
1977-06-24
Sponsor / Applicant
Combe, Inc.

Technical Specification

510(k) Submission ID K770413
Product Code EHS
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3540
Decision Date 1977-06-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CUSHIONS, DENTURE ADHESIVE, ALL-DAY received FDA 510(k) clearance under submission number K770413, sponsored by Combe, 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 1977-06-24.

Classification & Regulation

This clearance is catalogued under FDA product code EHS and 21 CFR 872.3540, within the Dental review panel as a Class II device.