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ULTRATEMP FIRM, FAST AND REGULAR SET

K080768 Class II Special
Decision Date
2008-04-11
Sponsor / Applicant
Ultradent Products, Inc.

Technical Specification

510(k) Submission ID K080768
Product Code EMA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3275
Decision Date 2008-04-11
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ULTRATEMP FIRM, FAST AND REGULAR SET received FDA 510(k) clearance under submission number K080768, sponsored by Ultradent Products, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2008-04-11.

Classification & Regulation

This clearance is catalogued under FDA product code EMA and 21 CFR 872.3275, within the Dental review panel as a Class II device.