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NUPRO PROPHYLAXIS PASTE WITH FLUORIDE AND TRICLOSAN

K000169 Class I Traditional
Decision Date
2000-03-24
Sponsor / Applicant
Dentsply Intl.

Technical Specification

510(k) Submission ID K000169
Product Code EJR
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6030
Decision Date 2000-03-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NUPRO PROPHYLAXIS PASTE WITH FLUORIDE AND TRICLOSAN received FDA 510(k) clearance under submission number K000169, 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 2000-03-24.

Classification & Regulation

This clearance is catalogued under FDA product code EJR and 21 CFR 872.6030, within the Dental review panel as a Class I device.