meddevicedb.com FDA Device Reference

RADIOTHERAPY TREATMENT

K790134 Class II Traditional
Decision Date
1979-02-21
Sponsor / Applicant
General Electric Co.

Technical Specification

510(k) Submission ID K790134
Product Code JAK
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1750
Decision Date 1979-02-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RADIOTHERAPY TREATMENT received FDA 510(k) clearance under submission number K790134, sponsored by General Electric Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1979-02-21.

Classification & Regulation

This clearance is catalogued under FDA product code JAK and 21 CFR 892.1750, within the Radiology review panel as a Class II device.