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9.6% HYDROFLUORIC ACID GEL

K896655 Class II Traditional
Decision Date
1990-02-14
Sponsor / Applicant
Pulpdent Corp.

Technical Specification

510(k) Submission ID K896655
Product Code KLE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3200
Decision Date 1990-02-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

9.6% HYDROFLUORIC ACID GEL received FDA 510(k) clearance under submission number K896655, 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 1990-02-14.

Classification & Regulation

This clearance is catalogued under FDA product code KLE and 21 CFR 872.3200, within the Dental review panel as a Class II device.