meddevicedb.com FDA Device Reference

CAMERA, CLEON 720 LARGE FIELD GAMMA

K790081 Class I Traditional
Decision Date
1979-01-26
Sponsor / Applicant
Union Carbide Corp.

Technical Specification

510(k) Submission ID K790081
Product Code IYX
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1100
Decision Date 1979-01-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CAMERA, CLEON 720 LARGE FIELD GAMMA received FDA 510(k) clearance under submission number K790081, sponsored by Union Carbide Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1979-01-26.

Classification & Regulation

This clearance is catalogued under FDA product code IYX and 21 CFR 892.1100, within the Radiology review panel as a Class I device.