K243299
- 510(k) number
- K243299
- Device name
- ACUSON Redwood Diagnostic Ultrasound System
- Applicant
- Siemens Medical Solutions USA, Inc. WA · US
- Product code
- IYN — System, Imaging, Pulsed Doppler, Ultrasonic
- Decision date
- 2024-11-15
- Date received
- 2024-10-18
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Flag
- Third-party review
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K243299.pdf
Official FDA record: K243299
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.