meddevicedb.com FDA Device Reference

PANTOS, MODELS: PANTOS 16, AND PANTOS DG

K031801 Class II Traditional
Decision Date
2003-09-11
Sponsor / Applicant
Blue X Imaging Srl

Technical Specification

510(k) Submission ID K031801
Product Code MUH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.1800
Decision Date 2003-09-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PANTOS, MODELS: PANTOS 16, AND PANTOS DG received FDA 510(k) clearance under submission number K031801, sponsored by Blue X Imaging Srl. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2003-09-11.

Classification & Regulation

This clearance is catalogued under FDA product code MUH and 21 CFR 872.1800, within the Dental review panel as a Class II device.