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. Device class: 2.
Clearance details
- Applicant
- Philips Ultrasound, LLC
- Product code
- Code QIH
- Device class
- Class 2
- Regulation
- 21 CFR 892.2050
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Bothell, WA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.