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FDA 510(k)

Spectral CT Verida Family

K-Number: K253649 · 2026-03-27

ApplicantPhilips Medical Systems Technologies , Ltd.
Decision Date2026-03-27
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Spectral CT Verida Family is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems Technologies , Ltd.. It received FDA 510(k) clearance on 2026-03-27 under 510(k) number K253649. 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 Spectral CT Verida Family?

Spectral CT Verida Family is a medical device that received FDA 510(k) clearance on 2026-03-27. The listed applicant is Philips Medical Systems Technologies , Ltd.. The 510(k) number is K253649.

When did Spectral CT Verida Family receive FDA 510(k) clearance?

Spectral CT Verida Family received FDA 510(k) clearance on 2026-03-27, under 510(k) number K253649.

Who is the listed applicant for Spectral CT Verida Family?

The FDA 510(k) record lists Philips Medical Systems Technologies , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Spectral CT Verida Family?

The FDA product code for Spectral CT Verida Family is JAK.

Other records listing Philips Medical Systems Technologies , Ltd. 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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Official Source

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

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