meddevicedb.com FDA Device Reference

PAPAYA PLUS, DIGITAL EXTRAORAL SOURCE X-RAY SYSTEM

K130419 Class II Traditional
Decision Date
2013-11-06
Sponsor / Applicant
Genoray Co., Ltd.

Technical Specification

510(k) Submission ID K130419
Product Code MUH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.1800
Decision Date 2013-11-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PAPAYA PLUS, DIGITAL EXTRAORAL SOURCE X-RAY SYSTEM received FDA 510(k) clearance under submission number K130419, sponsored by Genoray Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2013-11-06.

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.