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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 the device name listed in this FDA 510(k) record. The listed applicant is Philips Ultrasound, LLC. It received FDA 510(k) clearance on 2025-02-10 under 510(k) 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. The listed applicant is Philips Ultrasound, LLC. The 510(k) number is K241659.

When did Ultrasound Workspace (UWS 6.0) receive FDA 510(k) clearance?

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

Who is the listed applicant for Ultrasound Workspace (UWS 6.0)?

The FDA 510(k) record lists Philips Ultrasound, LLC as the applicant. This does not by itself establish the device manufacturer.

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

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

Other records listing Philips Ultrasound, LLC as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: QIH)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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