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PULPDENT ETCH-RITE ROYALE

K031915 Class II Traditional
Decision Date
2003-08-05
Sponsor / Applicant
Pulpdent Corporation

Technical Specification

510(k) Submission ID K031915
Product Code KLE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3200
Decision Date 2003-08-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PULPDENT ETCH-RITE ROYALE received FDA 510(k) clearance under submission number K031915, sponsored by Pulpdent Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2003-08-05.

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.