meddevicedb.com FDA Device Reference

Real Time Image Gating System for Proton Beam Therapy Systems

K171049 Class II Traditional
Decision Date
2017-12-26
Sponsor / Applicant
Hitachi, Ltd. Healthcare

Technical Specification

510(k) Submission ID K171049
Product Code LHN
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5050
Decision Date 2017-12-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Real Time Image Gating System for Proton Beam Therapy Systems received FDA 510(k) clearance under submission number K171049, sponsored by Hitachi, Ltd. Healthcare. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2017-12-26.

Classification & Regulation

This clearance is catalogued under FDA product code LHN and 21 CFR 892.5050, within the Radiology review panel as a Class II device.