K260123
- 510(k) number
- K260123
- Device name
- EPIQ Series Diagnostic Ultrasound System
- Applicant
- Philips Ultrasound, LLC WA · US
- Product code
- IYN — System, Imaging, Pulsed Doppler, Ultrasonic
- Decision date
- 2026-05-27
- Date received
- 2026-01-15
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K260123.pdf
Official FDA record: K260123
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.