Ultrasound Workspace (UWS 6.0)— 510(k) K241659
Substantially EquivalentPhilips Ultrasound, LLC
FDA 510(k) clearance K241659 for Ultrasound Workspace (UWS 6.0), Substantially Equivalent on 2025-02-10. Applicant: Philips Ultrasound, LLC.
Clearance details
- Applicant
- Philips Ultrasound, LLC
- Product code
- Code QIH
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Bothell, WA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.