ANGIO-CT MIYABI— 510(k) K990491
Substantially EquivalentSiemens Medical Solutions USA, Inc.
FDA 510(k) clearance K990491 for ANGIO-CT MIYABI, Substantially Equivalent on 1999-04-05. Applicant: Siemens Medical Solutions USA, Inc.. Device class: 2.
Clearance details
- Applicant
- Siemens Medical Solutions USA, Inc.
- Product code
- Code IXI
- Device class
- Class 2
- Regulation
- 21 CFR 892.5710
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Iselin, NJ, US
Recent devices under product code IXI
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