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RESIN TOOTH BONDING AGENT

K994302 Class II Traditional
Decision Date
2000-02-07
Sponsor / Applicant
Parkell, Inc.

Technical Specification

510(k) Submission ID K994302
Product Code KLE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3200
Decision Date 2000-02-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RESIN TOOTH BONDING AGENT received FDA 510(k) clearance under submission number K994302, sponsored by Parkell, 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 2000-02-07.

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.