K260667
- 510(k) number
- K260667
- Device name
- Alturion Series Diagnostic Ultrasound System
- Applicant
- Philips Ultrasound, LLC WA · US
- Product code
- IYN — System, Imaging, Pulsed Doppler, Ultrasonic
- Decision date
- 2026-06-29
- Date received
- 2026-03-02
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K260667.pdf
Official FDA record: K260667
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.