Symbia T16, Symbia Intevo 16 and Symbia Intevo Bold— 510(k) K173023
Substantially EquivalentSiemens Medical Solutions USA, Inc.
FDA 510(k) clearance K173023 for Symbia T16, Symbia Intevo 16 and Symbia Intevo Bold, Substantially Equivalent on 2017-11-17. Applicant: Siemens Medical Solutions USA, Inc.. Device class: 2.
Clearance details
- Applicant
- Siemens Medical Solutions USA, Inc.
- Product code
- Code KPS
- Device class
- Class 2
- Regulation
- 21 CFR 892.1200
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Hoffman Estates, IL, US
Recent devices under product code KPS
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