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Prodigio Stain Powder

K171167 Class II Traditional
Decision Date
2017-12-13
Sponsor / Applicant
Operart, LLC

Technical Specification

510(k) Submission ID K171167
Product Code EIH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6660
Decision Date 2017-12-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Prodigio Stain Powder received FDA 510(k) clearance under submission number K171167, sponsored by Operart, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2017-12-13.

Classification & Regulation

This clearance is catalogued under FDA product code EIH and 21 CFR 872.6660, within the Dental review panel as a Class II device.