meddevicedb.com FDA Device Reference

4% ACIDULATED PHOSPHATE FLUORIDE ETCHING GEL

K920460 Class II Traditional
Decision Date
1992-04-28
Sponsor / Applicant
Pulpdent Corp.

Technical Specification

510(k) Submission ID K920460
Product Code ELL
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3920
Decision Date 1992-04-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

4% ACIDULATED PHOSPHATE FLUORIDE ETCHING GEL received FDA 510(k) clearance under submission number K920460, sponsored by Pulpdent Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1992-04-28.

Classification & Regulation

This clearance is catalogued under FDA product code ELL and 21 CFR 872.3920, within the Dental review panel as a Class II device.