510(k) K252304

Device
syngo.via RT Image Suite VC10
Applicant
Varian Medical Systems, Inc.
510(k) number
K252304
Product code
MUJ
Decision
Substantially Equivalent (SESE)
Decision date
2026-03-18
Date received
2025-07-24
Regulation
892.5050
Classification name
System, Planning, Radiation Therapy Treatment
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Lynn Allman
Address
3100 Hansen Way Palo Alto CA US 94304 94304

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

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