K250886
- 510(k) number
- K250886
- Device name
- EPIQ Series Diagnostic Ultrasound Systems; Affiniti Series Diagnostic Ultrasound Systems
- Applicant
- Philips Ultrasound, LLC WA · US
- Product code
- IYN — System, Imaging, Pulsed Doppler, Ultrasonic
- Decision date
- 2025-06-18
- Date received
- 2025-03-25
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K250886.pdf
Official FDA record: K250886
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.