meddevicedb.com FDA Device Reference

NEW DENTINE ADHESIVE

K931812 Class II Traditional
Decision Date
1993-07-08
Sponsor / Applicant
Dentsply Intl.

Technical Specification

510(k) Submission ID K931812
Product Code KLE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3200
Decision Date 1993-07-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NEW DENTINE ADHESIVE received FDA 510(k) clearance under submission number K931812, sponsored by Dentsply Intl.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1993-07-08.

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.