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VITA ENAMIC STAINS

K123761 Class II Traditional
Decision Date
2013-03-01
Sponsor / Applicant
Innovation Meditech GmbH

Technical Specification

510(k) Submission ID K123761
Product Code EBD
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3310
Decision Date 2013-03-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VITA ENAMIC STAINS received FDA 510(k) clearance under submission number K123761, sponsored by Innovation Meditech GmbH. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2013-03-01.

Classification & Regulation

This clearance is catalogued under FDA product code EBD and 21 CFR 872.3310, within the Dental review panel as a Class II device.