Syngo.via RT Image Suite

System, Planning, Radiation Therapy Treatment

Siemens Medical Solutions USA Inc.

The following data is part of a premarket notification filed by Siemens Medical Solutions Usa Inc. with the FDA for Syngo.via Rt Image Suite.

Pre-market Notification Details

Device IDK220783
510k NumberK220783
Device Name:Syngo.via RT Image Suite
ClassificationSystem, Planning, Radiation Therapy Treatment
Applicant Siemens Medical Solutions USA Inc. 810 Innovation Drive Knoxville,  TN  37932
ContactClayton Ginn
CorrespondentClayton Ginn
Siemens Medical Solutions USA Inc. 810 Innovation Drive Knoxville,  TN  37932
Product CodeMUJ  
CFR Regulation Number892.5050 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeSpecial
3rd Party ReviewedNo
Combination ProductNo
Date Received2022-03-17
Decision Date2022-09-07

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