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PULPDENT SEALANT/PASTE ORTHODONTIC BRACKET ADHESIVE SYSTEM

K020115 Class II Traditional
Decision Date
2002-02-28
Sponsor / Applicant
Pulpdent Corp.

Technical Specification

510(k) Submission ID K020115
Product Code DYH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3750
Decision Date 2002-02-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PULPDENT SEALANT/PASTE ORTHODONTIC BRACKET ADHESIVE SYSTEM received FDA 510(k) clearance under submission number K020115, sponsored by Pulpdent Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2002-02-28.

Classification & Regulation

This clearance is catalogued under FDA product code DYH and 21 CFR 872.3750, within the Dental review panel as a Class II device.