syngo.via RT Image Suite— 510(k) K232799
Substantially EquivalentSiemens Medical Solutions USA, Inc.
FDA 510(k) clearance K232799 for syngo.via RT Image Suite, Substantially Equivalent on 2024-04-26. Applicant: Siemens Medical Solutions USA, Inc.. Device class: 2.
Clearance details
- Applicant
- Siemens Medical Solutions USA, Inc.
- Product code
- 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
- Knoxville, TN, US
Recent devices under product code MUJ
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