meddevicedb.com FDA Device Reference

VINTAGE MP PRESS OVER

K122614 Class II Traditional
Decision Date
2013-05-16
Sponsor / Applicant
Shofu Dental Corporation

Technical Specification

510(k) Submission ID K122614
Product Code EIH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6660
Decision Date 2013-05-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VINTAGE MP PRESS OVER received FDA 510(k) clearance under submission number K122614, 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 2013-05-16.

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.