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ECLIPSE BONDING AGENT

K051707 Class II Special
Decision Date
2005-07-15
Sponsor / Applicant
Dentsply Intl.

Technical Specification

510(k) Submission ID K051707
Product Code KLE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3200
Decision Date 2005-07-15
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ECLIPSE BONDING AGENT received FDA 510(k) clearance under submission number K051707, sponsored by Dentsply Intl.. The device was reviewed via the Special premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2005-07-15.

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.