FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

syngo.via RT Image Suite VC10

K Number: K252304 · Decision Mar 18, 2026
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
255
Applicant Total
170
Review Days
237

Basic Information

Device Name
syngo.via RT Image Suite VC10
K Number
K252304
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Varian Medical Systems, Inc.
Date Received
July 24, 2025
Decision Date
March 18, 2026
Product Code
MUJ
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MUJ System, Planning, Radiation Therapy Treatment

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