K232145
- 510(k) number
- K232145
- Device name
- ACUSON Sequoia Diagnostic Ultrasound System, ACUSON Sequoia Select Diagnostic Ultrasound System, ACUSON Origin Diagnostic Ultrasound System
- Applicant
- Siemens Medical Solutions USA, Inc. WA · US
- Product code
- IYN — System, Imaging, Pulsed Doppler, Ultrasonic
- Decision date
- 2023-10-30
- Date received
- 2023-07-19
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
510(k) Summary (official FDA PDF): K232145.pdf
Official FDA record: K232145
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.