meddevicedb.com FDA Device Reference

X-VIEW

K024186 Class II Traditional
Decision Date
2004-04-01
Sponsor / Applicant
Sometech Corporation

Technical Specification

510(k) Submission ID K024186
Product Code MUH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.1800
Decision Date 2004-04-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

X-VIEW received FDA 510(k) clearance under submission number K024186, sponsored by Sometech 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 2004-04-01.

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.