meddevicedb.com FDA Device Reference

ETCH AND BOND

K852660 Class II Traditional
Decision Date
1985-07-25
Sponsor / Applicant
Dentsply Intl.

Technical Specification

510(k) Submission ID K852660
Product Code KLE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3200
Decision Date 1985-07-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ETCH AND BOND received FDA 510(k) clearance under submission number K852660, 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 1985-07-25.

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.