Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

syngo.via RT Image Suite

K-Number: K220783 · 2022-09-07

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2022-09-07
Product CodeMUJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

syngo.via RT Image Suite is a medical device manufactured by Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2022-09-07 under approval number K220783. 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?

syngo.via RT Image Suite is a medical device that received FDA 510(k) clearance on 2022-09-07. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K220783.

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

syngo.via RT Image Suite received FDA 510(k) clearance on 2022-09-07, under approval number K220783.

What company makes syngo.via RT Image Suite?

syngo.via RT Image Suite is manufactured by Siemens Medical Solutions USA, Inc..

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

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

Related Clinical Trials

NCT07263815 EQUIP - Evaluation of Quality of Imaging on a Next-generation Total Body Pet Scan in Comparison to Conventional PET ACTIVE_NOT_RECRUITING

Other Devices by Siemens Medical Solutions USA, Inc.

K162302Somatom Confidence ® RT Pro K162971Multix Fusion Max K161795MAGNETOM ESSENZA K162541syngo Application Software K162736Biograph Horizon PET/CT and Biograph mCT PET/CT and Biograph mCT Flow PET/CT K162370syngo.via RT Image Suite

View all 248 devices →

Related Devices (Code: MUJ)

K162370syngo.via RT Image SuiteSiemens Medical Solutions USA, Inc. K161136Precision Treatment Planning SystemAccuray Incorporated K160093RayStationRaySearch Laboratories AB (PUBL) K151435MRCATPhilips Medical Systems MR Finland K153368Radiance V3Gmv Soluciones Globales Internet S.A.U. K170750RT Elements, Cranial SRS, Spine SRS, Multiple Brain Mets SRS, RT QA, Adaptive Hybrid Surgery Analysis, Dose ReviewBrainlab AG

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.

↑