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FDA 510(k)

CT:VQ

K-Number: K251484 · 2025-08-28

Applicant4Dmedical Limited
Decision Date2025-08-28
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CT:VQ is the device name listed in this FDA 510(k) record. The listed applicant is 4Dmedical Limited. It received FDA 510(k) clearance on 2025-08-28 under 510(k) number K251484. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CT:VQ?

CT:VQ is a medical device that received FDA 510(k) clearance on 2025-08-28. The listed applicant is 4Dmedical Limited. The 510(k) number is K251484.

When did CT:VQ receive FDA 510(k) clearance?

CT:VQ received FDA 510(k) clearance on 2025-08-28, under 510(k) number K251484.

Who is the listed applicant for CT:VQ?

The FDA 510(k) record lists 4Dmedical Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CT:VQ?

The FDA product code for CT:VQ is JAK.

Other records listing 4Dmedical Limited 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.

K232392CT Lung Ventilation Analysis Software (CT:V)

Related Devices (Code: JAK)

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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