meddevicedb.com FDA Device Reference

Z-RAY INTRA-ORAL DIGITAL RADIOGRAPHY SYSTEM

K133206 Class II Traditional
Decision Date
2014-05-13
Sponsor / Applicant
Zuma Dental, LLC

Technical Specification

510(k) Submission ID K133206
Product Code MUH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.1800
Decision Date 2014-05-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Z-RAY INTRA-ORAL DIGITAL RADIOGRAPHY SYSTEM received FDA 510(k) clearance under submission number K133206, sponsored by Zuma Dental, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2014-05-13.

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.