meddevicedb.com FDA Device Reference

IMAGE-X 70 INTRAORAL X-RAY SYSTEM

K930761 Class II Traditional
Decision Date
1993-05-25
Sponsor / Applicant
Afp Imaging Corp.

Technical Specification

510(k) Submission ID K930761
Product Code EAP
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.1810
Decision Date 1993-05-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IMAGE-X 70 INTRAORAL X-RAY SYSTEM received FDA 510(k) clearance under submission number K930761, sponsored by Afp Imaging Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1993-05-25.

Classification & Regulation

This clearance is catalogued under FDA product code EAP and 21 CFR 872.1810, within the Dental review panel as a Class II device.