meddevicedb.com FDA Device Reference

HEMA-BENZ

K953405 Class II Traditional
Decision Date
1995-09-27
Sponsor / Applicant
Health-Dent Intl., Inc.

Technical Specification

510(k) Submission ID K953405
Product Code KLE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3200
Decision Date 1995-09-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEMA-BENZ received FDA 510(k) clearance under submission number K953405, sponsored by Health-Dent Intl., 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 1995-09-27.

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.