Spectral CT Verida Family
K-Number: K253649 · 2026-03-27
Decision Date2026-03-27
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Spectral CT Verida Family is a medical device manufactured by Philips Medical Systems Technologies , Ltd.. It received FDA 510(k) clearance on 2026-03-27 under approval 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. It is manufactured by Philips Medical Systems Technologies , Ltd.. The 510(k) number is K253649.
When was Spectral CT Verida Family approved by the FDA?
Spectral CT Verida Family received FDA 510(k) clearance on 2026-03-27, under approval number K253649.
What company makes Spectral CT Verida Family?
Spectral CT Verida Family is manufactured by Philips Medical Systems Technologies , Ltd..
What is the FDA product code for Spectral CT Verida Family?
The FDA product code for Spectral CT Verida Family is JAK.
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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.