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Eclipse Treatment Planning System

K172163 Class II Special
Decision Date
2017-08-15
Sponsor / Applicant
Varian Medical Systems, Inc.

Technical Specification

510(k) Submission ID K172163
Product Code MUJ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5050
Decision Date 2017-08-15
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Eclipse Treatment Planning System received FDA 510(k) clearance under submission number K172163, sponsored by Varian Medical Systems, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2017-08-15.

Classification & Regulation

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