syngo.via RT Image Suite VC10— 510(k) K252304
Substantially EquivalentVarian Medical Systems, Inc.
FDA 510(k) clearance K252304 for syngo.via RT Image Suite VC10, Substantially Equivalent on 2026-03-18. Applicant: Varian Medical Systems, Inc.. Device class: 2.
Summary
Varian Medical Systems' syngo.via RT Image Suite VC10 is filed under MUJ, radiation therapy treatment planning systems. The record doesn't describe the product beyond its name and that code name.
Class II, 21 CFR 892.5050. Radiology is both the classification panel and the review panel. It was a Traditional 510(k).
Varian Medical Systems filed from Palo Alto, California. The decision came 237 calendar days after receipt (July 24, 2025 to March 18, 2026).
Clearance details
- Applicant
- Varian Medical Systems, Inc.
- Product code
- Product code MUJ
- Device class
- Class 2
- Regulation
- 21 CFR 892.5050
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Palo Alto, CA, US
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