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TRIPTON(TM) VISIBLE LIGHT-CURED UNIV. BONDING

K885010 Class II Traditional
Decision Date
1989-02-13
Sponsor / Applicant
Coe Laboratories, Inc.

Technical Specification

510(k) Submission ID K885010
Product Code KLE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3200
Decision Date 1989-02-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TRIPTON(TM) VISIBLE LIGHT-CURED UNIV. BONDING received FDA 510(k) clearance under submission number K885010, sponsored by Coe Laboratories, 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 1989-02-13.

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.