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FDA 510(k)

Ultrasound Workspace (UWS 6.0)

K-Number: K241659 · 2025-02-10

ApplicantPhilips Ultrasound, LLC
Decision Date2025-02-10
Product CodeQIH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Ultrasound Workspace (UWS 6.0) is a medical device manufactured by Philips Ultrasound, LLC. It received FDA 510(k) clearance on 2025-02-10 under approval number K241659. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Ultrasound Workspace (UWS 6.0)?

Ultrasound Workspace (UWS 6.0) is a medical device that received FDA 510(k) clearance on 2025-02-10. It is manufactured by Philips Ultrasound, LLC. The 510(k) number is K241659.

When was Ultrasound Workspace (UWS 6.0) approved by the FDA?

Ultrasound Workspace (UWS 6.0) received FDA 510(k) clearance on 2025-02-10, under approval number K241659.

What company makes Ultrasound Workspace (UWS 6.0)?

Ultrasound Workspace (UWS 6.0) is manufactured by Philips Ultrasound, LLC.

What is the FDA product code for Ultrasound Workspace (UWS 6.0)?

The FDA product code for Ultrasound Workspace (UWS 6.0) is QIH.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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