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NUPRO SENSODYNE PROPHYLAXIS PASTE WITH NOVAMIN

K121698 Class I Traditional
Decision Date
2012-08-06
Sponsor / Applicant
Dentsply International, Inc.

Technical Specification

510(k) Submission ID K121698
Product Code EJR
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6030
Decision Date 2012-08-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NUPRO SENSODYNE PROPHYLAXIS PASTE WITH NOVAMIN received FDA 510(k) clearance under submission number K121698, sponsored by Dentsply International, 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 2012-08-06.

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.