meddevicedb.com FDA Device Reference

GX-770 X-RAY CONTROL, MODEL 46-404600G4

K935046 Class II Traditional
Decision Date
1994-02-18
Sponsor / Applicant
Gendex Corp.

Technical Specification

510(k) Submission ID K935046
Product Code EHD
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.1800
Decision Date 1994-02-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GX-770 X-RAY CONTROL, MODEL 46-404600G4 received FDA 510(k) clearance under submission number K935046, sponsored by Gendex 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 1994-02-18.

Classification & Regulation

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