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VERACIA SA

K113426 Class II Traditional
Decision Date
2012-02-08
Sponsor / Applicant
Shofu Dental Corporation

Technical Specification

510(k) Submission ID K113426
Product Code ELM
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3590
Decision Date 2012-02-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VERACIA SA received FDA 510(k) clearance under submission number K113426, sponsored by Shofu Dental 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 2012-02-08.

Classification & Regulation

This clearance is catalogued under FDA product code ELM and 21 CFR 872.3590, within the Dental review panel as a Class II device.