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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 the device name listed in this FDA 510(k) record. The listed applicant is Varian Medical Systems, Inc.. It received FDA 510(k) clearance on 2026-03-18 under 510(k) 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. The listed applicant is Varian Medical Systems, Inc.. The 510(k) number is K252304.

When did syngo.via RT Image Suite VC10 receive FDA 510(k) clearance?

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

Who is the listed applicant for syngo.via RT Image Suite VC10?

The FDA 510(k) record lists Varian Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

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.

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Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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