meddevicedb.com FDA Device Reference

VINTAGE PRO

K181496 Class II Traditional
Decision Date
2018-12-18
Sponsor / Applicant
Shofu Dental Corporation

Technical Specification

510(k) Submission ID K181496
Product Code EIH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6660
Decision Date 2018-12-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VINTAGE PRO received FDA 510(k) clearance under submission number K181496, 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 2018-12-18.

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.