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FDA 510(k)

syngo.via RT Image Suite VC10

K-Number: K252304 · 2026-03-18

ApplicantVarian Medical Systems, Inc.
Decision Date2026-03-18
Product CodeMUJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

syngo.via RT Image Suite VC10 is a medical device manufactured by Varian Medical Systems, Inc.. It received FDA 510(k) clearance on 2026-03-18 under approval number K252304. The device is classified under product code MUJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the syngo.via RT Image Suite VC10?

syngo.via RT Image Suite VC10 is a medical device that received FDA 510(k) clearance on 2026-03-18. It is manufactured by Varian Medical Systems, Inc.. The 510(k) number is K252304.

When was syngo.via RT Image Suite VC10 approved by the FDA?

syngo.via RT Image Suite VC10 received FDA 510(k) clearance on 2026-03-18, under approval number K252304.

What company makes syngo.via RT Image Suite VC10?

syngo.via RT Image Suite VC10 is manufactured by Varian Medical Systems, Inc..

What is the FDA product code for syngo.via RT Image Suite VC10?

The FDA product code for syngo.via RT Image Suite VC10 is MUJ.

Related Clinical Trials

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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