meddevicedb.com FDA Device Reference

ALGI-BAND

K951237 Class II Traditional
Decision Date
1995-04-10
Sponsor / Applicant
Health-Dent Intl., Inc.

Technical Specification

510(k) Submission ID K951237
Product Code ELW
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3660
Decision Date 1995-04-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ALGI-BAND received FDA 510(k) clearance under submission number K951237, 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 1995-04-10.

Classification & Regulation

This clearance is catalogued under FDA product code ELW and 21 CFR 872.3660, within the Dental review panel as a Class II device.