meddevicedb.com FDA Device Reference

DINABASE (TM)

K971138 Class II Traditional
Decision Date
1997-07-21
Sponsor / Applicant
Sultan Chemists, Inc.

Technical Specification

510(k) Submission ID K971138
Product Code EBI
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3760
Decision Date 1997-07-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DINABASE (TM) received FDA 510(k) clearance under submission number K971138, sponsored by Sultan Chemists, 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 1997-07-21.

Classification & Regulation

This clearance is catalogued under FDA product code EBI and 21 CFR 872.3760, within the Dental review panel as a Class II device.